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F. W. Lichtenthaler: List of Publications

2011 − 2006 1995 − 1991 1980 − 1976
2005 − 2001 1990 − 1986 1975 − 1971
2000 − 1996 1985 − 1981 1970 − 1958

Please note: The copyrights to these publications are held by their publishers, hence the PDF-files provided here may be used as single copies for personal use only, as if they were reprints provided by mail. They may not be reposted on other web sites or used for any other purpose without the express permission of the appropriate publishers.

2011
303. F. W. Lichtenthaler:
2-Oxoglycosyl ("Ulosyl") and 2-Oximinoglycosyl Bromides: Versatile Donors for the Expedient Assembly of Oligosaccharides with β-D-Mannose, β-L-Rhamnose, N-Acetyl-β-D-mannosamine, and N-Acetyl-β-D-mannosaminuronic Acid Units.
Chem. Rev. 2011, 111, 5569–5609.
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302. T. Nakagawa, F. W. Lichtenthaler:
Sugar-Derived Building Blocks, 45. − Convenient access to 4-O-glycosylated 1,5-anhydro-D-fructoses via disaccharide-derived 2-hydroxyglycal esters.
Tetrahedron: Asymmetry 2011, 22, 740–744.
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301. F. W. Lichtenthaler:
Carbohydrates as Organic Raw Materials.
Ullmann's Encyclopedia of Industrial Chemistry, 7th Edition, Release 2011, 35pp. (Download PDF-File)
300. F. W. Lichtenthaler:
Carbohydrates: Occurrence, Structures and Chemistry.
Ullmann's Encyclopedia of Industrial Chemistry, 7th Edition, Release 2011, 30pp. (Download PDF-File)
2009
299. M. Lergenmüller, U. Kläres, F. W. Lichtenthaler:
Sugar-Derived Building Blocks, 44. − E versus Z geometry in β-D-arabino-hexopyranosidulose oximes.
Carbohydr. Res. 2009, 344, 2127-2136.
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298. P. Jarglis, V. Göckel, F. W. Lichtenthaler
Sugar-Derived Building Blocks, 43. − A convenient access to the 1,5-anhydro forms of D-tagatose, L-rhamnulose and D-xylulose via 2-hydroxyglycal esters.
Tetrahedron: Asymmetry 2009, 20, 952–960.
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2008
297. M. Brehm, V. H. Göckel, P. Jarglis, F. W. Lichtenthaler:
Sugar Derived Building Blocks, 42. − Expedient Conversions of D-Glucose into 1,5-Anhydro-D-fructose and into single-stereogenic-center Dihydropyranones, suitable six-carbon Scaffolds for the concise Syntheses of the Soft-coral Constituents Bissetone und Palythazine.
Tetrahedron: Asymmetry 2008, 19, 358-372.
(Download PDF-File)
296. F. W. Lichtenthaler:
Industrial Chemicals from Carbohydrate Feedstocks: Current Status and Challenges Ahead.
In Production of Fuels, Specialty Chemicals and Biobased Products from Agro-industrial Waste.
(F. Fava, P. Canepa, Eds.), INCA (Interuniversitario Nazionale Chimica Ambiente), Venezia, 2008, 230-253.
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2007
295. M. Lergenmüller, F. W. Lichtenthaler:
Sugar-Derived Building Blocks, 41. – Glucuronic Acid-Based Ulosyl Donors.
Carbohydr. Res. 2007, 342, 2132-2137.
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294. A. Benz, F. W. Lichtenthaler:
On the Alkoxybromination of Glucal Esters: 2-Acetamido-α-D-mannosyl Bromides from 2-Acetamidoglucal.
Tetrahedron: Asymmetry 2007, 18, 1108-1114
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293. F. W. Lichtenthaler:
Carbohydrates as Renewable Raw Materials: A Major Challenge of Green Chemistry.
In Methods and Reagents for Green Chemistry: An Introduction (P. Tundo, A. Perosa, F. Zecchini, Eds.), J. Wiley, Hoboken, NJ, 2007, pp. 23-63.
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2006
292. E. Cuny, S. Mondel, F. W. Lichtenthaler:
Sugar-Derived Building Blocks, 40. − Novel Polyamides from Disaccharide-Derived Dicarboxylic Acids.
Internat. Carbohydr. Symp., Whistler, CAN 2006, Abstr. TUE. PS 12.
paper292.pdf
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291. E. Cuny, F. W. Lichtenthaler:
Sugar-Derived Building Blocks, 39. − A Concise Stereocontrolled Synthesis of Spectinomycin.
Tetrahedron: Asymmetry 2006, 17, 1120-1124.
(Download PDF-File)
290. F. W. Lichtenthaler:
The Key Sugars of Biomass: Availability, Present Non-Food Applications and Potential Industrial Development Lines.
In Biorefineries, Biobased Industrial Processes and Products (B. Kamm, P. Gruber, M. Kamm, Eds.), Wiley-VCH, Weinheim, 2006, Vol. 2, pp. 3-59.
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289. D. Martin, F. W. Lichtenthaler:
Sugar-Derived Building Blocks, 38. − Glycosylated Hydroxymethylfurfurals.
Tetrahedron: Asymmetry 2006, 17, 756-762.
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2005
288. F. W. Lichtenthaler, E. Cuny, O. Sakanaka:
Sugar-Derived Building Blocks, 37. − An Efficient and General Method for Doubly Attaching 2-Ketosugars to Aglycon Diols: Synthesis of the Gomphosides and of Spectinomycin.
Angew. Chem. 2005, 117, 5024-5028.
Angew. Chem. Int. Ed. Engl. 2005, 44, 4944-4948.
(Download PDF-File; Supporting Information)
2004
287. F. W. Lichtenthaler:
Carbohydrates as Biofeedstocks for the Chemical Industry.
Green Chemistry Series No. 1 (P. Tundo, Ed.), 3rd Ed., INCA (Interuniversitario Nazionale Chimica Ambiente), Venezia, 2004, pp. 105-127.
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286. F. W. Lichtenthaler, E. Cuny:
Sugar-Derived Building Blocks, 36. − Linear Fused Pyran-Dioxane-Cyclohexane Tricycles: Synthesis of Five Linkage Isomers and Ensuing Reactions.
Eur. J. Org. Chem. 2004, 4911-4920.
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285. E. Cuny, F. W. Lichtenthaler, H. J. Lindner:
Sugar-Derived Building Blocks, 35. − Pyrano-dioxanes via Bis-acetalic Annulation of 2-Ketosugars to Vicinal Diols.
Eur. J. Org. Chem. 2004, 4901-4910.
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284. F. W. Lichtenthaler, T. Weimer, S. Immel:
Sugar-Derived Building Blocks, 34. − [4+2] and [2+2] Photocycloadditions of 1,2-Diketones to Glycal and Hydroxyglycal Esters.
Tetrahedron: Asymmetry 2004, 15, 2703-2709.
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283. A. Boettcher, F. W. Lichtenthaler:
Sugar-Derived Building Blocks, 33. − D-Fructose- and L-Sorbose-derived endo- and exo-Hydroxyglycal Esters and Some of their Chemistry.
Tetrahedron: Asymmetry 2004, 15, 2693-2701.
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282. F. W. Lichtenthaler, S. Peters:
Sugar-Derived Building Blocks, 32. − Carbohydrates as Green Raw Materials for the Chemical Industry.
Comptes Rendus Chimie 2004, 7, 65-90.
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2003
281. F. W. Lichtenthaler, J. Klotz, K. Nakamura:
Sugar-Derived Building Blocks, 31. − (-)-Daucic Acid: Proof of D-lyxo Configuration, Synthesis of D-ribo, D-xylo, L-arabino, and L-lyxoAnalogs, and Biosynthetic Implications.
Tetrahedron: Asymmetry 2003, 14, 3973-3986.
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280. S. Peters, F. W. Lichtenthaler, H. J. Lindner:
Sugar-Derived Building Blocks, 30. − A 2-C-Fructosyl-propanone Locked in a 2,7-Dioxabicyclo[3.2.1]octane Frame.
Tetrahedron: Asymmetry 2003, 14, 2475-2479.
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279. F. W. Lichtenthaler, M. Lergenmüller, S. Schwidetzky:
Sugar-Derived Building Blocks, 29. − C-Glycosidations of Ulosyl Bromides via Electrophilic, Radical and Nucleophilic Anomeric Carbons.
Eur. J. Org. Chem. 2003, 3094-3103.
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278. H. J. Lindner, D-Q. Yuan, K. Fujita, F. W. Lichtenthaler:
Crystal Structure of Mono-[3-(2-imidazolylthio)]-altro-β-cyclodextrin: Elliptical Distortion of the Macrocycle and Unique 'Yin-Yang' Stacking.
Chem. Commun. 2003, 1730-1731.
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277. F. W. Lichtenthaler, H. J. Lindner, K. Fujita, D-Q. Yuan, Y. Ren:
Guest Differentiation in a 6I,6II-Disubstituted β-Cyclodextrin.
Acta Cryst. 2003, E59, o408-o411.
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276. F. W. Lichtenthaler, K. Nakamura, J. Klotz:
(-)-Daucic Acid: Revision of Configuration, Synthesis and Biosynthetic Implications.
Angew. Chem. 2003, 115, 6019-6023.
Angew. Chem. Int. Ed. Engl. 2003, 42, 5838-5843.
(Download PDF-File − German / Download PDF-File − English)
275. F. W. Lichtenthaler:
Das "Händige" am Hochzeitsturm.
TUD-intern 2003, 24(7), 7.
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274. F. W. Lichtenthaler, T. Metz:
Efficient Generation of β-L-Rhamnosidic Linkages via the Ulosyl Donor Approach. Synthesis of a Rhamnotriose with a Central β-L-Rhamnose Unit.
Eur. J. Org. 2003, 3081-3093.
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273. H. J. Lindner, F. W. Lichtenthaler, K. Fujita, C. Yang:
Per-(3-deoxy)-α-cyclomannin: A n-Butanol Hexahydrate Inclusion Complex.
Acta Cryst. 2003, E59, o387-o389.
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272. F.W. Lichtenthaler, M. Lergenmüller, S. Peters, Z. Varga:
Manno- versus gluco-Selectivity in Reductions of 2-Keto-β-D-arabino-hexopyranosides.
Tetrahedron: Asymmetry 2003, 14, 727-736.
(Download PDF-File)
271. F.W. Lichtenthaler:
Sugar-Derived Building Blocks for the Synthesis of Non-Carbohydrate Natural Products.
In: Carbohydrate Synthons in Natural Products Chemistry (Z. J. Witczak, K. Tatsuta, Eds.), ACS Symposium Series Nr. 841, Washington, DC, 2003, pp. 47-83.
(Download PDF-File)
270. L. Jaenicke, F.W. Lichtenthaler:
Ein Kaiser-Wilhelm-Institut für Köln! Emil Fischer, Konrad Adenauer und die Meirowsky-Stiftung.
Angew. Chem. 2003, 115, 746-750.
Angew. Chem. Int. Ed. Engl. 2003, 42, 722-726.
(Download PDF-File − German / Download PDF-File − English)
2002
269. F.W. Lichtenthaler:
Emil Fischer, his Personality, his Achievements, and his Scientific Progeny.
Eur. J. Org. Chem. 2002, 4095-4122.
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268. F.W. Lichtenthaler:
Emil Fischer und die Entwicklung der Organischen Chemie in Ungarn.
Humboldt-Berichte Ungarn, 2002, No. 22, 4-12.
(Download PDF-File)
267. F.W. Lichtenthaler:
Emil Fischer und seine Schule.
Nachr. Chem. 2002, 50, 1342-1345.
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"Emil Fischer és Iskolája" (Hungarian Translation)
Magyar Kémikusok Lapja (Hung. J. Chem.) 2003, 177-180)
266. F.W. Lichtenthaler:
The Carbohydrates.
Ullmann's Encyclopedia Industrial Chemistry,6th Edn., 2002, 6, 237-279.
(Download PDF-File)
265. J. Thompson, F.W. Lichtenthaler, S. Peters, A. Pikis:
β-Glucoside Kinase from Klebsiella pneumoniae: Expression, Purification, Homology, and Preparative Synthesis of 6-Phospho-β-D-glucosides.
J. Biol. Chem. 2002, 277, 34310-34321.
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264. M. Oberthür, S. Peters, S. K. Das, F.W. Lichtenthaler:
Synthesis of Linear β(1→4)-galacto-Hexa- and Heptasaccharides and Studies Directed towards Cyclogalactans.
Carbohydr. Res. 2002, 337, 2171-2180.
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263. F. W. Lichtenthaler:
Sugar-Derived Building Blocks, 27. − Unsaturated O- and N-Heterocycles from Carbohydrate Feedstocks.
Acc. Chem. Res. 2002, 35, 728-737.
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2001
262. J.A. Barnett, F.W. Lichtenthaler:
A History of Research on Yeasts 3: Emil Fischer, Eduard Buchner and their Contemporaries, 1880-1900.
Yeast 2001, 18, 363-388.
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261. S. Immel, F. W. Lichtenthaler, H. J. Lindner, T. Nakagawa:
Molecular Modeling of Saccharides, 29. − Hydroxymethyl-substituted Crown Acetals with 35-C-14 and 40-C-16 Skeletal Backbones: Synthesis and Molecular Geometries.
Tetrahedron: Asymmetry 2001, 12, 2767-2774.
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260. F.W. Lichtenthaler, A. Brust, E. Cuny:
Sugar-Derived Building Blocks, 26. − Hydrophilic Pyrroles, Pyridazines, and Diazepinones from D-Fructose and Isomaltulose.
Green Chemistry 2001, 3, 201-209.
(Download PDF-File)
259. J. Thompson, S.A. Robrish, S. Immel, F.W. Lichtenthaler, B.G. Hall, A. Pikis:
Metabolism of Sucrose and its Five Linkage-isomeric α-D-Glucosyl-D-fructoses by Klebsiella pneumoniae: Participation and properties of Sucrose-6-phosphate Hydrolase and Phospho-α-glucosidase.
J. Biol. Chem. 2001, 276, 37415-37425.
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258. F.W. Lichtenthaler, M. Oberthür, S. Peters:
Directed and Efficient Synthesis of β(1→4)-Linked Galacto-oligosaccharides.
Eur. J. Org. Chem. 2001, 3849-3869.
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257. J. Thompson, S.A. Robrish, A. Pikis, A. Brust, F.W. Lichtenthaler:
Phosphorylation and metabolism of sucrose and its five linkage-isomeric α-D-glucosyl-D-fructoses by Klebsiella pneumoniae.
Carbohydr. Res. 2001, 331, 149-161.
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2000
256. T. Nakagawa, S. Immel, H.J. Lindner, F.W. Lichtenthaler:
Large Ring Crown Acetals from Cyclodextrins.
Cyclodextrin: From Basic Research to Market (Eds.: G. Schmidt, J. Szejtli), Wacker Biochem. Corp., Ann Arbor, MI, 2000, pp. 420-425.
Abstract
255. S. Immel, T. Nakagawa, H.J. Lindner, F.W. Lichtenthaler:
Molecular Modeling of Saccharides, 27. − Synthesis and Molecular Geometry of an Achiral 30-Crown-12 Polyacetal from α-Cyclodextrin.
Chem. Eur. J. 2000, 6, 3366-3371.
254. S. Immel, F. W. Lichtenthaler, H. J. Lindner, K. Fujita, M. Fukudome, Y. Nogami:
Molecular Modeling of Saccharides, 26. − The 2,3-Anhydro-α-cyclomannin - 1-Propanol Hexahydrate: Topography, Lipophilicity Pattern, and Solid-state Architecture.
Tetrahedron: Asymmetry 2000, 11, 27-36.
(Download PDF-File)
253. S. Immel, K. Fujita, H. J. Lindner, Y. Nogami, F. W. Lichtenthaler:
Molecular Modeling of Saccharides, 25. − Structure and Lipophilicity Profile of 2,3-Anhydro-α-cyclomannin and its Ethanol Inclusion Complex.
Chem. Eur. J. 2000, 6, 2327-2333.
252. S. Immel, F. W. Lichtenthaler:
Molecular Modeling of Saccharides, 24. − The Hydrophobic Topographies of Amylose and its Blue Iodine Complex.
Starch/Stärke 2000, 52, 1-8.
251. T. Nakagawa, S. Immel, F. W. Lichtenthaler, H. J. Lindner:
Molecular Modeling of Saccharides, 23. − Topography of a 1:1 α-Cyclodextrin - Nitromethane Inclusion Complex.
Carbohydr. Res. 2000, 324, 141-146.
1999
250. F. W. Lichtenthaler:
From Rigid Cyclodextrins to Flexible Non-glucose Cyclooligosaccharides.
Proceedings 17thCyclodextrin Symp. (Ed.: A. Harada), Osaka, 1999, Osaka Univ. Press 1999, pp. 41-46.
249. J.G. Zeidler, H.U. May, F.W. Lichtenthaler, H.K. Lichtenthaler:
Isoprene Emitted by Plants is Formed via the 1-Deoxy-D-xylulose Phosphate Pathway of Isopentenyl Diphosphate Biosynthesis.
In: Advances in PLant Lipid Research (Eds.: J. Sanchez, E. Cerda-Olmedo, E. Martinez-Force), Sevilla Univ. Publ., 1999, pp. 446-449.
248. C. Müller, S. Schwender, A. Disch, R. Rohmer, F.W. Lichtenthaler:
Occurence of the 1-Deoxy-D-xylulose 5-Phosphate Pathway of Isopentenyl Diphosphate Biosynthesis in Different Algae.
In: Advances in PLant Lipid Research (Eds.: J. Sanchez, E. Cerda-Olmedo, E. Martinez-Force), Sevilla Univ. Publ., 1999, pp. 425-428.
247. H. Gohlke, S. Immel, F.W. Lichtenthaler:
Molecular Modeling of Saccharides, 22. − Conformations and Lipophilicity Profiles of Some Cyclic β(1→3)- and β(1→6)-Linked Oligogalactofuranosides.
Carbohydr. Res. 1999, 321, 96-104.
246. S. Immel, K. Fujita, F.W. Lichtenthaler:
Molecular Modeling of Saccharides, 21. − Solution Geometries and Lipophilicity Patterns of α-Cycloaltrin.
Chem. Eur. J. 1999, 5, 3185-3192.
245. K. Fujita, W.-H. Chen, D.-Q. Yuan, Y. Nogami, T. Koga, T. Fujioka, K. Mihashi, S. Immel, F.W. Lichtenthaler:
Molecular Modeling of Saccharides, 20. − Guest-induced Conformational Change in a Flexible Host: Mono-altro-β-cyclodextrin.
Tetrahedron: Asymmetry 1999, 10, 1689-1696.
244. F.W. Lichtenthaler, B. Werner:
Sugar-Derived Building Blocks, 25. − 3,3'-Dideoxytrehaloses via Dimerization of 2-Hydroxyglycal Esters.
Carbohydr. Res. 1999, 319, 47-54.
1998
243. S. Immel, G.E. Schmitt, F.W. Lichtenthaler:
Molecular Modeling of Saccharides, 19. − Cyclofructins with six to ten β(1→2)-linked Fructofuranose Units: Geometries, Electrostatic Profiles, Lipophilicity Patterns and Potential for Inclusion Complexation.
Carbohydr. Res. 1998, 313, 91-105.
242. F.W. Lichtenthaler:
Enantiopure Building Blocks from Sugars, 24. − Towards Improving the Utility of Ketoses as Organic Raw Materials.
Carbohydr. Res. 1998, 313, 69-90.
Abstract
241. S. Immel, G.E. Schmitt, F.W. Lichtenthaler:
Molecular Modeling of Saccharides, 18. − α-Cycloaltrin: Conformation and Properties in Aqueous Solution.
Proceedings 9th Internat. Symp. on Cyclodextrins (Ed.: J.J. Torres Labandeira), Kluwer Acad. Publ., Dordrecht, NL, 1998, pp. 41-48.
Abstract
240. H. Gohlke, S. Immel, F.W. Lichtenthaler, G.E. Schmitt:
Molecular Modeling of Saccharides, 17. − Molecular Geometries of Furanoid β(1→3)- and β(1→6)-Linked Cyclogalactins.
Proceedings 9th Internat. Symp. on Cyclodextrins (Ed.: J.J. Torres Labandeira), Kluwer Acad. Publ., Dordrecht, NL, 1998, pp., 63-68.
Abstract
239. S. Immel, G.E. Schmitt, F.W. Lichtenthaler:
Molecular Modeling of Saccharides, 16. − The Molecular Geometries of Cyclofructins.
Proceedings 9th Internat. Symp. on Cyclodextrins (Ed.: J.J. Torres Labandeira), Kluwer Acad. Publ., Dordrecht, NL, 1998, pp. 57-62.
Abstract
238. F.W. Lichtenthaler, A. Vlach:
Industrially Viable Building Blocks from Ketoses? Status and Perspectives.
Proceedings 1998 Sugar Processing Research Conference, Savannah (Ed.: M.A. Clarke), SPRI Inc., New Orleans, 1998, pp. 109-126.
Abstract
237. C. Müller, V. Diehl, F.W. Lichtenthaler:
Building Blocks from Sugars, 23. − Hydrophilic 3-Pyridinols from D-Fructose and Isomaltulose.
Tetrahedron 1998, 54, 10703-10712.
Abstract
236. N. Oikawa, C. Müller, M. Kunz, F.W. Lichtenthaler:
Enantiopure Building Blocks from Sugars, 22. − Hydrophilically Functionalized Pyrazoles from Sugars.
Carbohydr. Res. 1998, 309, 269-279.
Abstract
235. V. Diehl, E. Cuny, F.W. Lichtenthaler:
Building Blocks from Sugars, 21. − Preparative Scale-Conversion of D-Xylose into Hydrophilically Functionalized Pyrazols.
Heterocycles 1998, 48, 1193-1201.
Abstract
234. F.W. Lichtenthaler, P. Pokinskyj:
Exploitation of Sucrose Chemistry towards Products with Industrial Application Profiles.
Carbohydrates as Organic Raw Materials IV (Eds.: W. Praznik, A. Huber), WUV Universitätsverlag, Wien, 1998, pp. 9-19.
Abstract
1997
233. F.W. Lichtenthaler, U.Kläres, Z. Szurmai, B. Werner:
4,6-Di-O-benzoyl-3-O-benzyl-α-D-arabino-hexopyranos-2-ulosyl Bromide: A Conveniently Accessible Glycosyl Donor for the Expedient Construction of Diantennary β-D-Mannosides Branched at O-3 and O-6.
Carbohydr. Res. 1997, 305, 293-303.
Abstract
232. J. Schwender, J. Zeidler, R. Gröner, C. Müller, M. Focke, S. Braun, F.W. Lichtenthaler, H.K. Lichtenthaler:
Incorporation of 1-Deoxy-D-xylulose into Isoprene and Phytol by Higher PLants anf Algae.
FEBS Lett. 1997, 414, 129-134.
Abstract
231. F.W. Lichtenthaler:
Carbohydrate Research at Darmstadt University of Technology
Carbohydrates in Europe 1997, 18, 8-17.
230. F.W. Lichtenthaler, T. Metz:
Efficient Generation of β-L-Rhamnosidic Linkages via the Ulosyl Bromide Approach.
Tetrahedron Lett. 1997, 38, 5477-5480.
Abstract
229. F.W. Lichtenthaler, S.Mondel:
manno- and altro-Sucrose and some Amino-Analogs.
Carbohydr. Res. 1997, 303, 293-302.
Abstract
228. Y. Nogami, K. Nasu, T. Koga, K. Ohta, K. Fujita, S. Immel, H.J. Lindner, G.E. Schmitt, F.W. Lichtenthaler:
Molecular Modeling of Saccharides, 15. Synthesis, Structure, and Conformational Features of α-Cycloaltrin: a Cyclooligosaccharide with alternating 4C1 and 1C4 Pyranoid Chairs.
Angew. Chem. 1997, 109, 1987-1991.
Angew. Chem. Int. Ed. Engl. 1997,35, 1899-1902.
Poster Eurocarb 9
227. F.W. Lichtenthaler, S. Mondel:
Enantiopure Building Blocks from Sugars, 20. Perspectives in the Use of Low Molecular Weight Carbohydrates as Organic Raw Materials.
Pure Appl. Chem. 1997, 69, 1853-1866.
Abstract
226. F.W. Lichtenthaler:
Exploitation of Sucrose Chemistry towards Products with Industrial Application Profiles.
Zuckerindustrie (Berlin) 1997, 122, 126.
225. J.G. Zeidler, H.K. Lichtenthaler, H.U. May, F.W. Lichtenthaler:
Is Isoprene Emitted by Plants Synthesized via a Novel Isopentenyl Pyrosphosphate Pathway?
Z. Naturforschg. 1997, 52c, 15-23.
Abstract
224. F.W. Lichtenthaler, S. Mondel:
Zucker als nachwachsender Rohstoff: über Molecular Modeling zu neuen Produkten mit industriellem Anwendungsprofil.
thema FORSCHUNG (Hrsg.: TH Darmstadt), Verlag für Kommunikation, Worms, 1997, 1, 90-98.
Abstract
223. T. Hanemann, E. Schumacher, W. Haase, F.W. Lichtenthaler:
Some Novel Disaccharide-derived Liquid Crystals.
Liquid Cryst. 1997, 22, 47-50.
Abstract
1996
222. F.W. Lichtenthaler, S. Immel:
Molecular Modeling of Saccharides, 14. The Lipophilicity Patterns of Cyclodextrins and of Non-glucose Cyclooligosaccharides.
J. Inclusion Phenom. Mol. Recognit. Chem. 1996, 25, 3-16.
Proceedings 8th Internat. Symp. on Cyclodextrins (Eds.: J. Szejtli, L. Szente), Kluwer Acad. Publ., Dordrecht/Boston, 1996, pp. 3-16.
Abstract
221. S. Immel, F.W. Lichtenthaler:
Molecular Modeling of Saccharides, 13. Permethylated α- and β-CD: Cyclodextrins with Inverse Hydrophobicity.
Starch/Stärke 1996, 48, 225-232.
Abstract
220. F.W. Lichtenthaler, P. Pokinskyj, S. Immel:
Molecular Modeling of Saccharides, 12. Sucrose as a Renewable Organic Raw Material: New, Selective Entry Reactions via Computersimulation of its Solution Conformations and its Hydroxyl Group Reactivities.
Zuckerindustrie (Berlin) 1996, 121, 174-190.
Abstract
219. F.W. Lichtenthaler, S. Immel:
Molecular Modeling of Saccharides, 11. Towards Understanding Formation and Stability of Cyclodextrin-Inclusion Complexes: Computation and Visualization of the Lipophilicity Patterns.
Starch/Stärke 1996, 48, 145-154.
Abstract
218. T. Hanemann, F.W. Lichtenthaler, W. Haase:
Complex New Liquid Crystalline Carbohydrates.
Polym. Materials Sci. Engineering 1996, 75, 215-216.
Abstract
217. P. Pokinskyj, S. Mondel, F.W. Lichtenthaler:
Über Molecular Modeling zu neuen Saccharose-Derivaten mit modifizierten Anwendungsprofilen. in Nachwachsende Rohstoffe: Perspektiven für die Chemie (Ed.: H. Eierdanz), VCH Publ., Weinheim/New York 1996, 295-298.
Abstract
216. A. Boettcher, J. Klotz, F.W. Lichtenthaler:
Studien an Ketosen, 13. Von Ketosen abgeleitete Zwischenprodukte mit industriellem Verwendungspotential.
in Nachwachsende Rohstoffe: Perspektiven für die Chemie (Ed.: H. Eierdanz), VCH Publ., Weinheim/New York 1996, 272-275.
Abstract
215. S. Immel, F.W. Lichtenthaler:
Molecular Modeling of Saccharides, 10. Studies on Ketoses, 12. -The Electrostatic and Lipophilic Potential Profiles of α-Cyclofructin: Computation, Visualization and Conclusions.
Liebigs Ann. 1996, 39-44.
Abstract
214. S. Immel, F.W. Lichtenthaler:
Molecular Modeling of Saccharides, 9. On the Hydrophobic Characteristics of Cyclodextrins: Computer-Aided Visualization of Molecular Lipophilicity Patterns.
Liebigs Ann. 1996, 27-37.
Abstract
1995
213. F.W. Lichtenthaler, S. Hahn, F.J. Flath:
Studies on Ketoses, 11. Enantiopure Building Blocks from Sugars, 19.
Pyranoid endo- and exo-Glycals from D- Fructose and L-Sorbose: Practical Routes for their Acquisition and Ensuing Reactions.
Liebigs Ann. Chem. 1995, 2081-2088.
Abstract
212. F.W. Lichtenthaler, J. Klotz, F.J. Flath:
Studies on Ketoses, 10. Acylation and Carbamoylation of D- Fructose: Acyclic, Furanoid and Pyranoid Derivatives and their Conformational Features.
Liebigs Ann. Chem. 1995, 2069-2080.
Abstract
211. F.W. Lichtenthaler, S. Immel, P. Pokinskyj:
Molecular Modeling of Saccharides, 8. Selective 2-O- Benzylation of Sucrose: A Facile Entry to its 2-Keto- and to 2- Deoxy-Derivatives, and to Sucrosamine.
Liebigs Ann. Chem. 1995, 1938-1947.
Abstract
210. S. Immel, F.W. Lichtenthaler:
Molecular Modeling of Saccharides, 7. The Conformation of Sucrose in Water: a Molecular Dynamics Approach.
Liebigs Ann. Chem. 1995, 1925-1937.
Abstract
209. E. Kaji, F.W. Lichtenthaler, Y. Osa, K. Takahashi, S. Zen:
A Practical Synthesis of Mannosaminyl-β(1→4)-glucosyl- α(1→2)-rhamnose, the Trisaccharide Repeating Unit of a Streptococcus pneumoniae Capsular Polysaccharide.
Bull. Chem. Soc. Jpn. 1995, 68, 2401- 2408.
Abstract
208. S. Immel, J. Brickmann, F.W. Lichtenthaler:
Molecular Modeling of Saccharides, 6. Small Ring Cyclodextrins: their Geometries and Hydrophobic Topographies.
Liebigs Ann. Chem. 1995, 929-942.
Abstract
207. E. Kaji, F.W. Lichtenthaler:
Expedient Conversion of Lactose into Versatile Derivatives of Lactosamine and Galactosyl-β(1→4)-mannosamine.
J. Carbohydr. Chem. 1995, 14, 791-803.
206. E. Kaji, F.W. Lichtenthaler, Y. Osa, S. Zen:
A Novel, Efficient Lactosaminyl Donor: N-Trichloroethoxycarbonyl- hexa-O-benzoyl-α-D-lactosaminyl Fluoride.
Bull. Chem. Soc. Jpn. 1995, 68, 1172- 1179.
205. A.M. Griffin, S. Schwidetzky, M.V.J. Ramsay, T. Gallagher, F.W. Lichtenthaler:
Reductive Cleavage as a Route to Carbohydrate Enolates. Applications to the Synthesis of C-linked Disaccharides.
J. Chem. Soc., Chem. Commun. 1995, 967-968.
204. F.W. Lichtenthaler, S. Immel:
Molecular Modeling of Saccharides, 5. Computersimulation of Chemical and Biological Properties of Sucrose, the Cyclodextrins, and Amylose.
Intern. Sugar J. 1995, 97, 12-22.
1994
203. F.W. Lichtenthaler, S. Immel:
Molecular Modeling of Saccharides, 4. Cyclodextrins, Cyclomannins and Cyclogalactins with five and six (1→4)-linked Sugar Units: Comparative Assessment of their Conformations and Hydrophobicity Potential Profiles.
Tetrahedron Asymmetry 1994, 5, 2045-2060.
202. F.W. Lichtenthaler:
100 Years "Schlüssel-Schloss-Prinzip": What made Emil Fischer use this Analogy?
Angew. Chem. 1994, 106, 2456-2467; Angew. Chem. Int. Ed. Engl. 1994, 33,
2364-2374.
201. F.W. Lichtenthaler:
Synthesebausteine aus Disacchariden.
Tagungsband 3. Symposium Nachwachsende Rohstoffe, Perspektiven für die Chemie, Schriftenreihe des Bundesministeriums für Ernährung, Landwirtschaft und Forsten, Landwirtschaftsverlag Münster, 1994, 149-165.
200. E. Cuny, F.W. Lichtenthaler, H.J. Lindner:
Molecular Geometry of a Pyrane-Dioxane-Cyclohexane Tricycle with Linear cis,trans-Fusion of Rings.
Acta Crystallogr. 1994, C50, 1599-1601.
199. F.W. Lichtenthaler:
Towards Understanding Chemical and Biological Properties of Sucrose, the Cyclodextrins, and Starch.
Proceedings, 1994 Sugar Processing Research Conference, Helsinki (M.A. Clarke, Ed.), S.P.R.I. Inc., New Orleans, Louisiana, 1994, 1-32.
198. E. Kaji, Y. Osa, K. Takahashi, M. Hirooka, S. Zen, F.W. Lichtenthaler:
Facile Preparation and Utilization of a Novel β-D-ManNAcA- Donor: Methyl 2-Benzoximino-1-bromo-α-D-arabino-hexopyranuronate.
Bull. Chem. Soc. Jpn. 1994, 67, 1130- 1140.
197. F.W. Lichtenthaler, T. Schneider-Adams, S. Immel:
A Practical Synthesis of β-D-Xyl-(1→2)-β-D-Man-(1→4)- β-D-Glc-OMe, a Trisaccharide Component of the Glycosphingolipid of Hyriopsis Schlegelii.
J. Org. Chem. 1994, 59, 6735-6738.
196. F.W. Lichtenthaler, T. Schneider-Adams:
3,4,6-Tri-O-benzyl-α-D-arabino-hexopyranos-2-ulosyl Bromide: A Glycosyl Donor for the Efficient Generation of β-D- Mannopyranosidic Linkages.
J. Org. Chem. 1994, 59, 6728-6734.
195. J. Dinges, F.W. Lichtenthaler, H.J. Lindner:
Molecular Structure of an O-Blocked Form of ACRL Toxin I.
Z. Kristallogr. 1994, 209, 512-513.
194. F.W. Lichtenthaler, H.J. Lindner, S. Rönninger, H. Paulus:
Enantiopure Building Blocks from Sugars, 18. Skew-boat Conformations for two Sugar-derived 5,6-Dihydropyran-2-ones.
Z. Kristallogr. 1994, 209, 274-277.
193. F.W. Lichtenthaler, B. Köhler:
An Expedient Route to Acylated Glucosyl Halides with a Free 2- OH Group.
Carbohydr. Res. 1994, 258, 77-85.
192. F.W. Lichtenthaler, F. Hoyer:
Studies on Ketoses, 9. Pyranoid D-Fructosyl and L-Sorbosyl Cyanides.
Carbohydr. Res. 1994, 253, 141-150.
1993
191. F.W. Lichtenthaler, R. Klimesch, V. Müller, M. Kunz:
Studies on Ketoses, 8. Enantiopure Building Blocks from Sugars, 17. Disaccharide Building Blocks from Isomaltulose: Glucosyl-α(1→5)-D-arabinonic Acid and Ensuing Products.
Liebigs Ann. Chem. 1993, 975-980.
190. F.W. Lichtenthaler, D. Martin, T. Weber, H. Schiweck:
Studies on Ketoses, 7. 5-(α-D-Glucosyloxymethyl)- furfural: Preparation from Isomaltulose and Exploitation of its Ensuing Chemistry.
Liebigs Ann. Chem. 1993, 967-974.
189. F.W. Lichtenthaler, S. Immel:
Molecular Modeling of Saccharides, 3. Studies on Ketoses, 6. Sucrose, Sucralose, and Fructose: Correlations between Hydrophobicity Potential Profiles and AH-B-X Assignments.
in Sweet Taste Chemoreception (M. Mathlouthi,
J. A. Kanters, G. G. Birch, Eds.), Elsevier Applied Science,
London/New York, 1993, 21-53.
188. F.W. Lichtenthaler, A. Boettcher:
Studien an Ketosen, 5. Zum Synthesepotential von Ketosen: Vielseitig verwendbare Zwischenprodukte aus D-Fructose, L-Sorbose und D-Isomaltulose.
in Nachwachsende Rohstoffe − Perspektiven für die Chemie (M. Eggersdorfer,
S. Warwel, G. Wulff, Eds.), VCH Publ., Weinheim/New York, 1993, 151-168.
187. Y. Fukuda, F.W. Lichtenthaler, H.J. Lindner, I. Svoboda:
Crystal Structure of the 1,5-Lactone of 5R,7S,9S,10-Tetrahydroxy- 7,9-di-O- isopropylidene-3-methoxy-8S-methyl-2-decenoic Acid, C15H24O 6.
Z. Kristallogr. 1993, 208, 246-248.
186. F.W. Lichtenthaler, S. Rönninger, H.J. Lindner, S. Immel, E. Cuny:
Enantiopure Building Blocks from Sugars, 16. Solid State Conformations of 2,6-cis- and 2,6-trans-substituted Dihydropyran-3-ones.
Carbohydr. Res. 1993, 249, 305-324.
185. Y. Osa, E. Kaji, T. Takahashi, M. Hirooka, F.W. Lichtenthaler, S. Zen:
Synthesis of a 2-Acetamido-2-deoxy-β-D-mannuronic Acid- containing Artificial Glycolipid Corresponding to a Repeating Unit of the Teichuronic Acid from Micrococcus luteus.
Chem. Lett. 1993, 1567-1570.
184. E. Kaji, F.W. Lichtenthaler:
2-Oxo- and 2-Oximinoglycosyl Halides: Versatile Glycosyl Donors for the Construction of β-D-Mannose and β-D- Mannosamine-containing Oligosaccharides.
Trends Glycosci. Glycotechnol. 1993, 5, 121-142.
1992
183. F.W. Lichtenthaler, S. Immel, D. Martin, V. Müller:
Some Disaccharide-derived Building Blocks of Potential Industrial Utility.
Starch/Stärke 1992, 44, 445-456.
Carbohydrates as Organic Raw Materials II (G. Descotes, Ed.),
VCH Publ., Weinheim/New York, 1993, 59-98.
182. F.W. Lichtenthaler:
Emil Fischer's Establishment of the Configuration of Sugars: A Centennial Tribute.
Angew. Chem. 1992, 104, 1577-1593;
Angew. Chem. Int. Ed. Engl. 1992, 31, 1541- 1556.
181. F.W. Lichtenthaler:
Enantiopure Building Blocks from Sugars (15), and their Utilization in Natural Product Synthesis. A Review with Procedures.
Modern Synthetic Methods (R. Scheffold, Ed.), VCH Publ., Weinheim/New York,
1992, 6, 273-376.
180. E. Kaji, F.W. Lichtenthaler, Y. Osa, K. Takahashi, E. Matsui, S. Zen:
A Practical, Highly Stereoselective Synthesis of the Trisaccharide Repeating Unit of a Streptococcus pneumoniae Polysaccharide.
Chem. Lett. 1992, 707-710.
179. F.W. Lichtenthaler:
Efficient Reaction Channels from Mono- and Disaccharides to Enantiopure Building Blocks, and Exploitation of their Application Profiles.
In Carbohydrates: Synthetic Methods and Applications in Medicinal Chemistry
(H. Ogura, A. Hasegawa, T. Suami, Eds.) Elsevier, Amsterdam, 1992, 3-27.
178. F.W. Lichtenthaler, U. Kläres, M. Lergenmüller, S. Schwidetzky:
Enantiopure Building Blocks from Sugars, 14. Various Glycosyl Donors with a Keto or Oximino Function next to the Anomeric Centre: Practical Preparation and Evaluation of their Selectivities in Glycosidations.
Synthesis 1992, 179-184.
1991
177. F.W. Lichtenthaler:
Molecular Modeling of Saccharides, 2. Perspektiven in der Nutzung niedermolekularer Kohlenhydrate als Rohstoffe für die Chemische Industrie.
Zuckerindustrie (Berlin) 1991, 116, 701- 712.
176. F.W. Lichtenthaler, S. Immel, U. Kreis:
Molecular Modeling of Saccharides, 1. The Structural Representation of Sucrose.
Starch/Stärke 1991, 43, 121-132.
Republished (in Japanese): Shokuhin Kogyo (The Food Industry) 1992, 35, 65-85.
175. F.W. Lichtenthaler, J. Dinges, Y. Fukuda:
Enantioreine Bausteine aus Zuckern, 13. ACRL Toxin I: Konvergente Totalsynthese des 3-Methylenolethers aus D-Glucose.
Angew. Chem. 1991, 103, 1385-1389;
Angew. Chem. Int. Ed. Engl. 1991, 30, 1339- 1343.
174. F.W. Lichtenthaler, E. Cuny, D. Martin, S. Rönninger, T. Weber:
Practical Routes from Mono- and Disaccharides to Building Blocks with Industrial Application Profiles.
in Carbohydrates as Organic Raw Materials (F.W. Lichtenthaler, Ed.), VCH Publ., Weinheim/New York, 1991, 207-246.
173. F.W. Lichtenthaler, S. Immel, U. Kreis:
Old Routes − New Branches: Evolution of the Structural Representation of Sucrose.
in Carbohydrates as Organic Raw Materials (Ed.: F.W. Lichtenthaler, Ed.), VCH
Publ., Weinheim/New York, 1991, 1- 32.
172. F.W. Lichtenthaler:
Carbohydrates as Organic Raw Materials. Monography developed from a Workshop Conference at the Technische Hochschule Darmstadt, April 12/13, 1990; VCH Publ., Weinheim/New York,
1991, 365 pp.
1990
171. F.W. Lichtenthaler:
Enantiopure Building Blocks from Sugars, 12. Large- scale Adaptable Routes from Mono- and Disaccharides to Building Blocks with Industrial Application Profiles.
Zuckerindustrie (Berlin) 1990, 115, 762-770.
170. F.W. Lichtenthaler, S. Rönninger, U. Kreis:
Tetra-O-acetyl-β-D-glucopyranosyl Chloride: Occurence of gg and gt Rotamers in the Crystal, and Correlation between Conformation at C-6 and Anomeric Stabilization.
Liebigs Ann. Chem. 1990, 1001-1006.
169. F.W. Lichtenthaler:
Niedermolekulare Kohlenhydrate als Rohstoffe für die Chemische Industrie.
Nachr. Chem. Tech. Lab. 1990, 38, 860- 864.
168. F.W. Lichtenthaler, S. Rönninger:
Studies on Ketoses, 4. α-D-Glucopyranosyl-D-fructoses: Distribution of Furanoid and Pyranoid Tautomers in Water, Dimethyl Sulphoxide, and Pyridine.
J. Chem. Soc., Perkin Trans.2, 1990, 1489-1497.
167. F.W. Lichtenthaler:
Large-Scale Adaptable Routes from Monosaccharides to Versatile Building Blocks.
Zuckerindustrie (Berlin) 1990, 115, 198.
166. W.G. Dauben, B.A. Kowalczyk, F.W. Lichtenthaler:
Enantiopure Building Blocks from Sugars, 11. Diels- Alder Reactions of Pyranoid Enolone Esters with Cyclopentadiene under Thermal Lewis Acid Catalysis, and High Pressure Conditions.
J. Org. Chem. 1990, 55, 2391-2398.
165. F.W. Lichtenthaler, H.J. Lindner:
On the Extent of Chair Distortion in "Tetraaxial" 2,3,4-Tri-O- benzoyl-β-D-xylopyranosyl Derivatives.
Carbohydr. Res. 1990, 200, 91-99.
164. F.W. Lichtenthaler, S. Schwidetzky, K. Nakamura:
Acylated 2-Oxo-glycosyl Bromides: Exploration of their Reaction Potential.
Tetrahedron Lett. 1990, 31, 71-74.
1989
163. F.W. Lichtenthaler, D. Martin, T.A. Weber, H.M. Schiweck:
5-(α-D-Glucopyranosyloxy)-furan-2-carboxaldehyd: Herstellung aus Isomaltulose und Folgereaktionen.
Dtsch. Offenl. DE 3.936.522 (Appl. 2 Nov 1989);
Eur. Pat. Appl. EP 426.176 (31 Oct 1990);
Chem. Abstr. 1991, 115, 92826t.
162. F.W. Lichtenthaler:
Enantiopure Building Blocks from Sugars: Efficient Preparation and Utilization in Natural Product Synthesis.
in New Aspects in Organic Chemistry I, (Z. Yoshida, T. Shiba, Y. Ohshiro, Eds.) VCH Publishers, Weinheim, New York, 1989, 351-384.
161. F.W. Lichtenthaler, S. Nishiyama, T. Weimer:
Enantiopure Building Blocks from Sugars, 10. 2,3- Dihydropyranones with Contiguous Chiral Centers: A Practical Route for their Acquisition and Evaluation of their Reaction Potential.
Liebigs Ann. Chem. 1989, 1163-1170.
160. F.W. Lichtenthaler, S. Rönninger, P. Jarglis:
Enantiopure Building Blocks from Sugars, 9. An Expedient Approach to Pyranoid Ene and Enol Lactones by BF3- Catalyzed Peroxidation of Glycal and Hydroxyglycal Esters.
Liebigs Ann. Chem. 1989, 1153-1161.
159. F.W. Lichtenthaler:
Enantioreine Synthesebausteine aus Kohlenhydraten.
Schriftenreihe, Fonds der Chemischen Industrie, 1988, 31, 94-105.
1988
158. D.R. Williams, F.D. Klingler, E.E. Allen, F.W. Lichtenthaler:
Bromine as an Oxidant for Direct Conversion of Aldehydes into Esters.
Tetrahedron Lett. 1988, 29, 5087-5090.
157. E. Kaji, F.W. Lichtenthaler, T. Nishino, A. Yamane, S. Zen:
Practical Syntheses of Immunologically Relevant β- Glycosides of 2-Acetamido-2-deoxy-D-mannopyranose: Methyl N-Acetyl- β-D-mannosaminide, N-Acetyl-mannosaminyl-β(1→6)-D- galactose, and Methyl N-Acetyl-mannosaminyl-β(1→6)-D-glucoside.
Bull. Chem. Soc. Jpn. 1988, 61, 1291- 1297.
156. F.W. Lichtenthaler, P. Jarglis, K. Lorenz:
Enantiopure Building Blocks from Sugars, 8. Convenient One-Pot Conversion of Alcohols into Esters via Hemiacetal Intermediates.
Synthesis 1988, 790-792.
1987
155. K. Lorenz, F.W. Lichtenthaler:
Enantiopure Building Blocks from Sugars, 6. A Convergent Total Synthesis of (+)-Anamarine from (R,R)-Tartrate and L- Gulonolactone.
Tetrahedron Lett. 1987, 28, 6437-6440.
154. W.Y. Ma, F.W. Lichtenthaler:
A Facile Synthesis of 1,2:5,6-Di-O-isopropylidene-α-D- hexofuranos-3-ulose.
Yiyao Gongye (Pharm. Ind.) 1987, 18, 67- 69; Chem. Abstr. 1987, 107, 217948c.
153. M. Brehm, W.G. Dauben, P. Köhler, F.W. Lichtenthaler:
Enantioreine Bausteine aus Zuckern, 5. Beweis der S,S-Konfiguration von (-)-Bisseton durch Synthese aus D- Glucose.
Angew. Chem. 1987, 99, 1318-1319. Angew. Chem. Int. Ed. Engl. 1987, 26, 1271-
1273.
152. F.W. Lichtenthaler:
Bemerkungen zu zwei Sofort-Mitteilungen von G. Oremek et al. über "Regioselektive Reduktion von Zucker-Enolonen" und deren "Katalytische Hydrierung".
Chemiker-Ztg. 1987, 111, 146-147.
151. F.W. Lichtenthaler, K.H. Neff:
"Carbohydrates 1987"
Abstracts of the 4th European Carbohydrate Symposium, Darmstadt, July 12-17,
1987; 400 pp. Published by Gesellschaft Deutscher Chemiker, 1987.
ISBN 3-924 763-14-3.
150. F.W. Lichtenthaler, A. Pashalidis, H.J. Lindner:
Studies on Ketoses, 3. Conversion of D-Fructose into 4-Amino-, 4-Amino-4-C-methyl-, and 3,4,5-Triamino-Derivatives of L-Sorbose.
Carbohydr. Res. 1987, 164, 357-372.
149. F.W. Lichtenthaler:
Karl Freudenberg, Burckhardt Helferich, and Hermann O. L. Fischer:
A Centennial Tribute.
Carbohydr. Res. 1987, 164, 1-22.
148. F.W. Lichtenthaler, K. Lorenz, W.Y. Ma:
Enantiomerically Pure Building Blocks from Sugars, 4. A Convergent Total Synthesis of (-)-Anamarine.
Tetrahedron Lett. 1987, 27, 47-50.
1986
147. F.W. Lichtenthaler:
Pyranoid Chiral Building Blocks: Preparation from Monosaccharides and Utilization for Natural Product Synthesis. (Enantiopure Building Blocks from Sugars, Part 1.)
In Natural Product Chemistry (Atta-ur-Rahman, Ed.),
Proceedings First Internat. Symp. Karachi, 1984, Springer,
Berlin/New York, 1986, pp. 227-254.
1985
146. F.W. Lichtenthaler, W. Doleschal, S. Hahn:
Enantiopure Building Blocks from Sugars, 3. Studies on Ketoses, 2.
Spirocyclic Dihydropyranones from D-Fructose.
Liebigs Ann. Chem. 1985, 2454-2464.
145. B. Schneider, F.W. Lichtenthaler, G. Steinle, H. Schiweck:
Studies on Ketoses, 1. Distribution of Furanoid and Pyranoid Tautomers of D-Fructose in Dimethylsulfoxide, Water and Pyridine via Anomeric Hydroxyl Proton NMR Intensities.
Liebigs Ann. Chem. 1985, 2443-2453.
144. F.W. Lichtenthaler, R.G. Klimesch:
Derivate und Reduktionsprodukte der D-Glucopyranosyl- α(1→5)-D-arabonsäure, deren Herstellung und Verwendung.
Ger. Offen. DE 3,248,404 (28 Dec 1982); US Pat. 4, 618 675 (16 Dec 1983);
Chem. Abstr. 1985, 102, 7034x.
143. F.W. Lichtenthaler, E. Kaji:
A Facile Access to Hetero-trisaccharides with Central α-D- Glucosamine, β-D-Mannose, and β-D-Mannosamine Units.
Liebigs Ann. Chem. 1985, 1659-1668.
142. F.W. Lichtenthaler, E. Kaji, S. Weprek:
Disaccharide-derived 2-Oxo- and 2-Oximino-glycosyl Bromides: Novel, Conveniently Accessible Building Blocks for the Expedient Construction of Oligosaccharides with α-D-Glucosamine, β-D- Mannose and β-D-Mannosamine as Constituent Sugars.
J. Org. Chem. 1985, 50, 3505-3515.
141. F.W. Lichtenthaler, S. Nishiyama, P. Köhler, and H.J.Lindner:
Sugar Enolones, XXI. Anomeric Stereocontrol in Addition Reactions of Hexose-derived Dihydropyranones.
Carbohydr. Res. 1985, 136, 13-26.
1984
140. F.W. Lichtenthaler, F.D. Klingler, P. Jarglis:
Enantiopure Building Blocks from Sugars, 2. Simple Synthesis of S-Parasorbic Acid and other (5S)- Hydroxy Six Carbon Synthons from L-Rhamnose.
Carbohydr. Res. 1984, 132, C1-C5.
1983
139. F.W. Lichtenthaler, E. Cuny, S. Weprek:
Zuckerenolone, XX. Eine einfache und leistungsfähige Synthese acylierter Glucosylbromide aus Hydroxylglycal-estern.
Angew. Chem. 1983, 95, 906; Angew. Chem. Int. Ed. Engl. 1983, 22, 891.
138. F.W. Lichtenthaler, A. Löhe, E. Cuny:
Sugar Enolones, XIX. An Approach to Actinospectose-Type 2,3- Diketo-sugars. Synthetic Proof for the R-Configuration of "Herzgift- Methylreduktinsäure".
Liebigs Ann. Chem. 1983, 1973-1985.
137. F.W. Lichtenthaler, P. Jarglis, W. Hempe:
Sugar Enolones, XVIII. Stereocontrolled Functionalization at Proanomeric Centres by Photobromination. A Novel Efficient Access to Oxo- and Oximinoglycosyl Bromides.
Liebigs Ann. Chem. 1983, 1959-1972.
1982
136. P. Jarglis, F.W. Lichtenthaler:
Zuckerenolone, XVII. Boron Trifluoride-catalyzed Oxidation of Glycal Esters: An Effective and Mild Method for their Conversion into α, β- Unsaturated Lactones.
Tetrahedron Lett. 1982, 23, 3781-3784.
135. F.W. Lichtenthaler, P. Jarglis:
Zuckerenolone, XVI. Funktionalisierung proanomerer Zentren durch Photobromierung. Ein neuer Zugang zu Oxo- und Oximino- glycosyl-bromiden.
Angew. Chem. 1982, 94, 643; Angew. Chem. Int. Ed. Engl. 1982, 21, 625;
Angew. Chem. Suppl. 1982, 1449-1459.
134. F.W. Lichtenthaler:
Disaccharidalkohole: Molekulare Geometrie und mögliche Beziehungen zwischen Konformation und Süsskraft.
Dtsch. Zahnärztl. Z. 1982, 37, S46-S49.
133. E. Cuny, F.W. Lichtenthaler, A. Moser:
Novel Pyrazoloquinazoline Derivatives and Methods of their Production.
US Pat. App. 152,527 (22 May 1980); Europ. Pat. 40872 (12 May 1981);
Chem. Abstr. 1982, 96, 142 882v.
132. P. Jarglis, F.W. Lichtenthaler:
Zuckerenolone, XV. Eine stereospezifische Synthese von S,S-Palythazin aus D-Glucose.
Angew. Chem. 1982, 94, 140-141; Angew. Chem. Int. Ed. Engl. 1982, 21,
141-142.

1981
131. L.A. Alexandrova, F.W. Lichtenthaler:
Nucleosides, 46. A New Synthesis of the Antibiotic Psicofuranine.
Nucleic Acids Res., Spec. Publ. 1981, 9, s263-s266.
130. F.W. Lichtenthaler, W. Eberhard, S. Braun:
Nucleosides, 45. Assignment of Glycosylation Sites in 5'-O-Hexopyranosyl-ribonucleosides by 13C-NMR.
Tetrahedron Lett. 1981, 22, 4401-4404.
129. F.W. Lichtenthaler, A. Moser:
Nucleosides, 44. Benzo-separated Pyrazolopyrimidines: Expeditious Syntheses of [3,4-g]- and [3,4-h]-linked Pyrazoloquinazolinones.
Tetrahedron Lett. 1981, 22, 4397-4400.
128. F.W. Lichtenthaler, H.J. Lindner:
The Preferred Conformations of Glycosyl-alditols.
Liebigs Ann. Chem. 1981, 2372-2383.
127. E. Cuny, W. Eberhard, F.W. Lichtenthaler:
Nucleosides, 43. Synthesis of Benzologously Extended Allopurinol Ribosides and Formycins.
Nucleic Acids Res., Spec. Publ. 1981, 9, s77-s81.
126. W. Eberhard, F.W. Lichtenthaler, K.A. Khan:
Nucleosides, 42. Galactopyranosyl-β(1→3')-ribonucleosides: Structural Evidence and Synthesis.
Nucleic Acids Res., Spec. Publ. 1981, 9, s15-s19.
125. H.J. Lindner, F.W. Lichtenthaler:
Extended Zigzag Conformation of 1-O-α-D- Glucopyranosyl-D-mannitol.
Carbohydr. Res. 1981, 93, 135-140.
124. B. Kraska, F.W. Lichtenthaler:
Nucleosides, 41. (1→5)-verknüpfte Glucopyranosyl-und Galactopyranosyl-ribosen.
Chem. Ber. 1981, 114, 1636-1648.
123. F.W. Lichtenthaler, E. Cuny:
Nucleosides, 40. Synthesis of a [3,4-f]-linked Pyrazoloquinazolinone.
Heterocycles 1981, 15, 1053-1059.
122. E. Cuny, F.W. Lichtenthaler, U. Jahn :
Nucleosides, 39. Angular und linear erweiterte Allopurinole: Pyrazolo[4,3-f] und [4,3-g]chinazolinone.
Chem. Ber. 1981, 114, 1624-1635.
121. F.W. Lichtenthaler, E. Cuny:
Nucleosides, 38. The Ribonucleosides of Allopurinol.
Chem. Ber. 1981, 114, 1610-1623.
1980
120. E. Cuny, F.W. Lichtenthaler, A. Moser:
Nucleosides, 37. Benzologs of Allopurinol: Synthesis of Pyrazolo[4,3-g] and [3,4-f]quinazolinones.
Tetrahedron Lett. 1980, 21, 3029-3032.
119. E. Cuny, F.W. Lichtenthaler:
Quinazoline Derivatives.
U.S. Pat. 4 223 143, 18 pp. (16 Sep 1980, Appl. 11 Dec 1978).
118. F.W. Lichtenthaler, E.S.H. El Ashry, V.H. Göckel:
Sugar Enolones, XIV, XIV. A Convenient Access to 1,5- Anhydroketoses.
Tetrahedron Lett. 1980, 21, 1429-1432.
117. F.W. Lichtenthaler, P. Jarglis:
Sugar Enolones, XIII. Selective Deacylation of Enol Esters with Hydroxylamine.
Tetrahedron Lett. 1980, 21, 1425-1428.
116. F.W. Lichtenthaler, P. Jarglis:
Sugar Enolones, XII. Peroxidation of Pyranose-derived Enolesters: An Efficacious Synthesis of Peracetyl-hexosuloses and their Conversion into gamma-Pyrones via 3,2-Enolones.
Chem. Ber. 1980, 113, 489-510.
115. F.W. Lichtenthaler, T. Sakakibara, E. Egert:
Sugar Enolones, XI. 2-Halopentopyranosyl Halides: Preparation, Configuration, Elucidation and Conversion into Enantiomeric Dihydropyranones.
Chem. Ber. 1980, 113, 471-488.
1979
114. F.W. Lichtenthaler, S. Nishiyama, P. Jarglis:
Zuckerenolone, X. Neuartige, hochstereoselektive Umlagerungen chiraler Dihydropyranone.
Angew. Chem. 1979, 91, 1001-1002; Angew. Chem. Int. Ed. Engl. 1979, 18, 936- 938.
113. F.W. Lichtenthaler, E. Cuny, T. Morino, I. Rychlík:
Nucleosides, XXXVI. Synthesis of 3'-Homocitrullylamino- and 3'- Lysylamino- 3'-deoxy-adenosine and their Relation to Cordyceps militaris-derived Products.
Chem. Ber. 1979, 112, 2588-2601.
112. F.W. Lichtenthaler, G. Bambach:
Monomeric Hexofuranoses with an Acetylimino Group in the Hemiacetal Ring.
Carbohydr. Res. 1979, 68, 305-312.
1978
111. F.W. Lichtenthaler:
Sugar Enolones, IX. Synthesis, Reactions of Preparative Interest and gamma-Pyrone Formation.
Pure Appl. Chem. 1978, 50, 1343-1362.
110. F.W. Lichtenthaler, Y. Sanemitsu, T. Nohara:
Nucleoside, XXXV. Synthese von O-Glucosyl- ribonucleosiden.
Angew. Chem. 1978, 90, 819-821; Angew. Chem. Int. Ed. Engl. 1978, 17, 772.
109. W. Riess, F.W. Lichtenthaler:
Nucleosides, XXXIV. Course and Scope of the Sugar Exchange Reaction in Purine Nucleosides.
Nucleic Acids Res., Spec. Publ. 1978, 4, s191-s194.
108. F.W. Lichtenthaler, K. Kitahara, W. Riess:
Nucleosides, XXXIII. N- versus O-Glycosylation of Purine Nucleosides.
Nucleic Acids Res., Spec. Publ. 1978, 4, s115-s118.
107. F.W. Lichtenthaler, U. Kraska, S. Ogawa:
Sugar Enolones, VIII. A Facile Preparation of Deoxy- hexosiduloses and Deoxy-hexosides.
Tetrahedron Lett. 1978, 1323-1326.
106. F.W. Lichtenthaler, K. Kitahara:
9-(3-Amino-3-deoxy-β-D-xylofurnosyl)hypoxanthine.
Nucleic Acid Chemistry: New or Improved Synthetic Procedures, Methods,
and Techniques, Part II, Wiley, New York 1978, pp. 547-552.
105. F.W. Lichtenthaler:
O'-Nitro Derivatives of Uridine: Preparation of Nitric Esters of Nucleosides.
Nucleic Acid Chemistry: Improved and New Synthetic Procedures, Methods,
and Techniques, Part I, Wiley, New York 1978, pp. 391-399.
1977
104. F.W. Lichtenthaler, S. Ogawa, P. Heidel:
Sugar Enolones, VII. Synthesis and gamma-Pyrone Formation of α,β-Unsaturated Hexopyranosid-4-uloses.
Chem. Ber. 1977, 110, 3324-3332.
103. F.W. Lichtenthaler, T. Sakakibara, E. Oeser:
Sugar Enolones, VI. Tetrabenzoyl-2-halo-hexopyranosyl Halides: Preparation, Assignment of Configuration and Hydrolysis to Enolones.
Carbohydr. Res. 1977, 59, 47-61.
102. F.W. Lichtenthaler, U. Kraska:
Sugar Enolones, V. Preparation and some Reactions of Benzoylated 4-Deoxy-D-glycero-hex-3-enosuloses.
Carbohydr. Res. 1977, 58, 363-377.
1976
101. F.W. Lichtenthaler, K. Strobel, G. Reidel:
Sugar Enolones, IV. Preparation and gamma-Pyrone Formation of Some Acylated 4-Deoxy-hex-3-enopyranosiduloses.
Carbohydr. Res. 1976, 49, 57-67.
100. F.W. Lichtenthaler, T. Kulikowski:
Nucleosides, XXXI. Synthesis of 1-(2,6-Dideoxy-β-D-arabino- hexopyranosyl)cytosine, the Nucleoside Portion of Oxamicetin.
J. Org. Chem. 1976, 41, 600-603.
1975
99. F.W. Lichtenthaler, K. Kitahara:
Nucleoside, XXXII. Austausch von Ribose gegen Glucose in Purin-Nucleosiden.
Angew. Chem. 1975, 87, 839-840; Angew. Chem. Int. Ed. Engl. 1975, 14, 815-816.
98. H. M. Menzel, F.W. Lichtenthaler:
Nucleosides, XXX. Structure-Activity Relationships in the Aminoacyl-4-aminohexosyl-cytosine Group of Peptidyl Tranferase Inhibitors.
Nucleic Acids Res., Spec. Publ. 1975, 1, s155-s158.
97. F.W. Lichtenthaler, T. Morino, W. Winterfeldt:
Nucleosides, XXIX. Total Synthesis of Aspiculamycin.
Nucleic Acid Res., Spec. Publ. 1975, 1, s33-s36.
96. E. Cuny, F.W. Lichtenthaler:
Nucleosides, XXVIII. Synthesis of Allopurinol-ribosides.
Nucleic Acids Res., Spec. Publ. 1975, 1, s25-s28.
95. K. Kitahara, B. Kraska, Y. Sanemitsu, F.W. Lichtenthaler:
Nucleosides, XXVII. Synthetic Approaches to O-Glycosyl- ribonucleosides.
Nucleic Acids Res., Spec. Publ. 1975, 1, s21-s24.
94. F.W. Lichtenthaler, T. Morino, W. Winterfeldt, Y. Sanemitsu:
Nucleosides, XXVI. An Alternate Synthetic Approach to Gougerotin.
Tetrahedron Lett. 1975, 3527-3530.
93. H. Paulsen, F.W. Lichtenthaler:
Chemie der Kohlenhydrate. Denkschrift über Entwicklung, gegenwärtigen Stand und absehbare zukünftige Entwicklungslinien.
H. Bott Verlag, Boppard, 94 S., 1975.
92. F.W. Lichtenthaler, H.J. Müller:
Ribonucleosid-5'-nitrate und Verfahren zu ihrer Herstellung.
Germ. Offen. DE 2 342 479 (13 Mar 1975, Appl. 28 Aug 1973);
Chem. Abstr. 1975, 83, 10732.
91. F.W. Lichtenthaler, T. Morino, H.M. Menzel:
Nucleosides, XXV. On the Structure of Aspiculamycin: its Identity with the Nucleoside Antibiotic Gougerotin.
Tetrahedron Lett. 1975, 665-668.
90. F.W. Lichtenthaler, J. Cerná, I. Rychlík:
Nucleosides, XXIV. The Effect of Oxamicetin and some Amicetin Analogs on Ribosomal Peptidyl Transferase.
Fed. Eur. Biochem. Soc. Lett. 1975, 53, 184-187.
1974
89. F.W. Lichtenthaler, K. Kitahara, K. Strobel:
Nucleosides, XXIII. A Simple Access to 3'-Amino-xylo- and 3',4'-unsaturated Purine Nucleosides.
Synthesis 1974, 860-862.
88. E. Fischer, F.W. Lichtenthaler:
Zuckerenolone, III. Ergiebige Synthese von Zucker-3,2-enolonen aus Hydroxyglycalen und ihre Umwandlung in gamma-Pyrone.
Angew. Chem. 1974, 86, 590-592; Angew. Chem. Int. Ed. Engl. 1974, 13, 546-548.
87. F.W. Lichtenthaler, E. Fischer:
1,2-Dichloride aus 2-Hydroxyglycalen: Darstellung und Konfigurationszuordnung anhand der Exciton Chiralitätsmethode.
Angew. Chem. 1974, 86, 592-594; Angew. Chem. Int. Ed. Engl. 1974, 13, 548-549.
86. F.W. Lichtenthaler, T. Ueno, P. Voss:
Nucleosides, XXII. Pyrimidine Nucleosides of 4-Amino-4-deoxy- β-D-galactopyranose.
Bull. Chem. Soc. Jap. 1974, 47, 2304.
85. F.W. Lichtenthaler, P. Voss, G. Bambach:
Nucleosides, XXI. Preparative Routes to Nucleosides derived from 4-Amino-4-deoxy-β-D-glucopyranose.
Bull. Chem. Soc. Jap. 1974, 47, 2297- 2303.
84. F.W. Lichtenthaler, P. Voss, A. Heerd:
Nucleosides, XX. Stannic Chloride-catalyzed Glycosidation of Silylated Purines with Fully Acylated Sugars.
Tetrahedron Lett. 1974, 2141-2144.
83. F.W. Lichtenthaler, P. Heidel:
Preparative Routes to 4-Amino-4-deoxy-D-galactose.
J. Org. Chem. 1974, 39, 1457-1462.
82. F.W. Lichtenthaler, A. Heerd, K. Strobel:
Nucleosides, XIX. Hexuronic Acid and Aminosugar Nucleosides via SnCl4-catalyzed Glycosidations of Silylpyrimidines with Peracyl Sugars.
Chemistry Lett. 1974, 449-452.
81. F.W. Lichtenthaler, H.J. Müller:
Nucleosides, XVIII. Improved Preparation of Nucleoside 5'-Nitrates.
Syntheses 1974, 199-201.
80. F.W. Lichtenthaler, G. Trummlitz:
Nucleosides, XVII. Structural Basis of Inhibition Protein Synthesis by the Aminoacyl Aminohexosyl Cytosine Group of Antibiotics.
Fed. Eur. Biochem. Soc. Lett. 1974, 38, 237-242.
1973
79. F. W. Lichtenthaler:
Cyclizing Additions of Methylene Components to Dialdehydes.
Kagaku (Kyoto) 1973, 28, 1032-1040.
78. T. Suami, S. Nishiyama, K. Tadano, F.W. Lichtenthaler:
Nucleosides, XVI. Synthesis of Carbocyclic Adenosine Analogs: 9-(2',3',4',5'-Tetrahydroxycyclopentyl)-adenines.
Bull. Chem. Soc. Jap. 1973, 46, 2562- 2564.
77. T. Suami, K. Tadano, S. Nishiyama, F.W. Lichtenthaler:
Aminocyclitols, 30. Unambiguous Synthesis of seven Amino-cyclopentanetetrols.
J. Org. Chem. 1973, 38, 3691-3696.
76. F.W. Lichtenthaler, H.J. Müller:
Nucleosides, XV. 5'-Nitrate von Pyrimidin-Nucleosiden: Salpetersäure-Analoge der Nucleotide.
Angew. Chem. 1973, 85, 765; Angew. Chem. Int. Ed. Engl. 1973, 12, 752-753.
75. J. Cerná, I. Rychlík, F.W. Lichtenthaler:
Nucleosides, XIV. The Effect of the Aminoacyl-4-amino-hexosyl- cytosine Group of Antibiotics on Ribosomal Peptidyl Transferase.
Fed. Eur. Biochem. Soc. Lett. 1973, 30, 147-150.
1972
74. F.W. Lichtenthaler, D. Fleischer:
Nitromethane Condensation with Dialdehydes, XX. Formation of Cyclohexane versa Tetrahydropyrane Derivatives on Reaction of Glutaraldehyde with Nitroalkanes.
J. Org. Chem. 1972, 37, 1670-1672.
73. F.W. Lichtenthaler, G. Bambach:
Nitromethane Condensations with Dialdehydes, XIX. C→O-Migration of an Ethoxycarbonyl Group.
J. Org. Chem. 1972, 37, 1621-1624.
72. F.W. Lichtenthaler, H. Zinke:
Nucleosides, XIII. Nitromethane Condensations with Dialdehydes, XVIII.
Synthesis and Interconversions of C- Methyl branched 1-(3-Amino-3-deoxy-β-D-hexopyranosyl)uracils. An Empirical Method for Configurational Assignments at the Branch Point by NMR.
J. Org. Chem. 1972, 37, 1612-1621.
71. F.W. Lichtenthaler:
Sugar Enolones, II. Unsaturated Glycopyranosiduloses.
Methods Carbohydr. Chem. 1972, 6, 348- 349.
70. F.W. Lichtenthaler:
Aminosugars and Aminocyclitols via Cyclization of Dialdehydes with Nitromethane.
Methods Carbohydr. Chem. 1972, 6, 250- 260.
1971
69. J. Cerná, F.W. Lichtenthaler, I. Rychlík:
Nucleosides, XII. The Effect of Gougerotin-Analogues on Ribosomal Peptidyl Transferase.
Fed. Eur. Biochem. Soc. Lett. 1971, 14, 45-48.
68. F.W. Lichtenthaler, G. Trummlitz, G. Bambach, I. Rychlík:
Nucleosides, XI. Synthese eines biologisch aktiven Gougerotin- Analogons.
Angew. Chem. 1971, 83, 331-332; Angew. Chem. Int. Ed. Engl. 1971, 10, 334-335.
67. F.W. Lichtenthaler, J. Breunig, W. Fischer:
Boron Trifluoride-catalyzed Acetolysis of Glycosides.
Tetrahedron Lett. 1971, 2825-2828.
1970
66. F.W. Lichtenthaler, W. Fischer:
2,3,4-Triamino-2,3,4-trideoxy Derivatives of 6-Deoxy-L- glucose and L-Rhamnose.
J. Chem. Soc. Chem. Comm. 1970, 1081.
65. T. Nakagawa, Y. Sato, T. Takamoto, F.W. Lichtenthaler:
Derivative der 2,3,4-Triamino-2,3,4- tridesoxy-β-D-glucopyranose.
Bull. Chem. Soc. Jap. 1970, 43, 3866- 3869.
64. T. Nakagawa, T. Sakakibara, F.W Lichtenthaler:
Modellreaktionen zur Aminierung cyclischer Nitrodiole.
Bull. Chem. Soc. Jap. 1970, 43, 3861- 3865.
63. F.W. Lichtenthaler, G. Trummlitz, P. Emig:
Nucleosides, X. Synthesis of Dipeptidyl Aminosugar Nucleosides Structurally Related to Gougerotin.
Tetrahedron Lett. 1970, 2061-2064.
62. F.W. Lichtenthaler:
Branched-chain Aminosugars and Aminocyclanols via Dialdehyde- Nitroalkane-Cyclization.
Fortschr. Chem. Forschg. 1970, 14, 556- 577.
1969
61. F.W. Lichtenthaler, P. Heidel:
Zuckerenolone, I. Zwischenprodukte der Bildung von gamma- Pyronenaus Hexose-Derivaten; eine einfache Synthese von Kojisäure und Hydroxymaltol.
Angew. Chem. 1969, 81, 998-999; Angew. Chem. Int. Ed. Engl. 1969, 8, 978-979.
60. F.W. Lichtenthaler, P. Voss:
as-Inosatriamine.
Tetrahedron Lett. 1969, 2297-2300.
59. F.W. Lichtenthaler, P. Voss, N. Majer:
Ein neuer Zugang zu Inosatriaminen und Triaminozuckern.
Angew. Chem. 1969, 81, 221-222; Angew. Chem. Int. Ed. Engl. 1969, 8, 211-212.
58. F.W. Lichtenthaler, G. Trummlitz, H. Zinke:
Nucleoside, IX. Synthese von Di- und Tri-aminozucker- Nucleosiden.
Tetrahedron Lett. 1969, 1213-1217.
57. F.W. Lichtenthaler, G. Bambach, P. Emig:
Nucleoside, VIII. Zur Konfigurationszuordnung von Zuckern und Hexopyranosyl-Nucleosiden mit Hilfe der Acetyl-Resonanzen-Regel.
Chem. Ber. 1969, 102, 994-1004.
56. F.W. Lichtenthaler, G. Bambach, U. Scheidegger:
Nucleoside, VII. Synthese und Konformation von 1-[3-amino-3- desoxy-β-D-galactopyranosyl]-uracil.
Chem. Ber. 1969, 102, 986-993.
55. F.W. Lichtenthaler, P. Emig, D. Bommer:
Nucleoside, VI. Nucleosid-Umwandlungen in der Reihe der 3'- Aminohexosyl-hypoxanthine.
Chem. Ber. 1969, 102, 971-985.
54. F.W. Lichtenthaler, H.P. Albrecht:
Nucleoside, V. 6-Dimethylaminopurin-Nucleoside der 3-Amino-3-desoxy- β-D-glucose, -mannose und -galactose.
Chem. Ber. 1969, 102, 964-970.
53. F.W. Lichtenthaler, N. Majer:
Nitromethan-Kondensation mit Dialdehyden, XVII. Cyclische Nitro-enamine.
Tetrahedron Lett. 1969, 411-414.
52. F.W. Lichtenthaler, P. Voss:
Nitromethan-Kondensation mit Dialdehyden, XVI. S- Benzylsubstituierte Nitrodithiole durch cyclisierende Bismerkapto-alkylierung von Nitromethanen.
Liebigs Ann. Chem. 1969, 724, 81-90.
1968
51. F.W. Lichtenthaler, P. Heidel:
Synthese von Derivaten der 4-Amino-4-desoxy-D-galactose.
Angew. Chem. 1968, 80, 441-442; Angew. Chem. Int. Ed. Engl. 1968, 7, 458-459.
50. F.W. Lichtenthaler, H.P. Albrecht:
Nucleoside, IV. Synthese eines Puromycin-Analogons.
Angew. Chem. 1968, 80, 440-441; Angew. Chem. Int. Ed. Engl. 1968, 7, 457-458.
49. T. Suami, F.W. Lichtenthaler, S. Ogawa, Y. Nakashima, H. Sano:
Aminocyclitols, XVII. A Facile Synthesis of 2-Deoxystreptamine.
Bull. Chem. Soc. Jap. 1968, 41, 1014- 1017.
48. F.W. Lichtenthaler, P. Emig:
NMR-Studien an Zuckern und Cyclanolen, V. Zusammenhang zwischen sterischer Orientierung von O- und N-Acetyl-Gruppen und der Signallage ihrer Methylresonanz bei Cyclit- und Amino-cyclit-polyacetaten.
Carbohydr. Res. 1968, 7, 121-137.
47. F.W. Lichtenthaler, T. Nakagawa:
Nitromethan-Kondensation mit Dialdehyden, XV. 2,3,4-Triamino- 2,3,4-tridesoxy-β-D-idosan.
Chem. Ber. 1968, 101, 1846-1849.
46. F.W. Lichtenthaler, T. Nakagawa, A. El Scherbiney:
Nitromethan-Kondensation mit Dialdehyden, XIV. Synthese cyclischer Nitrodiamine durch Bis-aminoalkylierung von Nitromethan.
Chem. Ber. 1968, 101, 1837-1845.
45. F.W. Lichtenthaler, H. Leinert, U. Scheidegger:
Nitromethan-Kondensation mit Dialdehyden, XIII. Zum sterischen Verlauf der Cyclisierung aliphatischer 1,5-Dialdehyde mit Nitromethylen-Verbindungen.
Chem. Ber. 1968, 101, 1819-1836.
44. F.W. Lichtenthaler, H. Leinert:
Nitromethan-Kondensation mit Dialdehyden, XII. Hydroxymethyl- verzweigte Cyclanole durch Dialdehyd-Cyclisierung mit 2- Nitroethanol.
Chem. Ber. 1968, 101, 1815-181.
43. F.W. Lichtenthaler, A. El Scherbiney:
Nitromethan-Kondensation mit Dialdehyden, XI. Zur Cyclisierung aromatischer Dialdehyde mit Methylen-Verbindungen.
Chem. Ber. 1968, 101, 1799-1814.
42. F.W. Lichtenthaler, H.K. Yahya:
NMR-Studien an Zuckern und Cyclanolen, IV. meta- Didesoxyinosamine.
Chem. Ber. 1968, 101, 908-915.
41. F.W. Lichtenthaler, H. Zinke:
The Dialdehydes Nitroethane Cyclization Applied to Nucleoside Dialdehydes: 1-(3-Amino-3-deoxy-3-C-methyl-β-D- glucopyranosyl)-uracil.
Synth. Procedures in Nucleic Acid Chem. 1968, 1, 366-368.
40. F.W. Lichtenthaler, H.P. Albrecht:
The Dialdehyde Nitromethane Cyclization applied to "Purine Nucleoside
Dialdehydes": 9-(β-D-Hexopyranosyl)-6-dimethylaminopurines derived from 3-Amino-3-deoxy-glucose, 3-Amino-3- deoxy-galactose, and 3-Amino-3-deoxy-mannose.
Synth. Procedures in Nucleic Acid Chem. 1968, 1, 253-257.
39. F.W. Lichtenthaler, P. Emig:
9-(3-Amino-3-deoxy-β-D-galactopyranosyl)-hypoxanthine.
Synth. Procedures in Nucleic Acid Chem. 1968, 1, 236-238.
38. F.W. Lichtenthaler, P. Emig:
Inversion at C-2 in 3-Amino-3-deoxy-aldopyranosyl-Nucleosides: 9-(Acetamido-3-deoxy-β-D-talopyranosyl)-hypoxanthine.
Synth. Procedures in Nucleic Acid Chem. 1978, 1, 232-235.
37. F.W. Lichtenthaler:
Cyclizations of Dialdehydes with Nitromethane. In Newer Methods of Preparative
Organic Chemistry (W. Först, Ed.), Vol. IV, 155-195, 1968.
Erweiterte Fassung der Deutschen Ausgabe Neue Methoden der präparativen
organischen Chemie (W. Först, Hrsg.), Bd. IV, S. 140-172, Verlag Chemie,
Weinheim 1966.
1967
36. F.W. Lichtenthaler, H. Leinert, T. Suami:
Eine einfache Synthese von Streptamin und Actinamin.
Chem. Ber. 1967, 100, 2383-2388.
35. T. Suami, F.W. Lichtenthaler, S. Ogawa:
Aminocyclitols, XI. Studies on the Synthesis of muco- Inosadiamines and an Inosatetramine.
Bull. Chem. Soc. Jap. 1967, 40, 1488- 1495.
34. F.W. Lichtenthaler, H.K. Yahya:
Nitromethan-Kondensation mit Dialdehyden, X. Synthese eines C-Methyl-verzweigten Inosamins.
Carbohydr. Res. 1967, 5, 485-489.
33. F.W. Lichtenthaler, T. Nakagawa, A. El Scherbiney:
Nitromethan-Kondensation mit Dialdehyden, X. Synthese cyclischer 1,2,3-Triamine durch Umsetzung von Dialdehyden mit Nitromethan und Benzylamin.
Angew. Chem. 1967, 79, 530-531; Angew. Chem. Int. Ed. Engl. 1967, 6, 568-569.
32. F.W. Lichtenthaler, H.K. Yahya:
Nitromethan-Kondensation mit Dialdehyden, VIII. 4-Nitro- und 4-Amino-Derivate der α-L-Sorbose und β-D-Tagatose.
Chem. Ber. 1967, 100, 2389-2400.
31. F.W. Lichtenthaler, H. P. Albrecht:
Nitromethan-Kondensation mit Dialdehyden, VII; Nucleoside III.Synthese von 2'-Nitro- und 3'-Amino-β-D-glucopyranosyl-thymin.
Chem. Ber. 1967, 100, 1845-1849.
30. F.W. Lichtenthaler, T. Nakagawa, J. Yoshimura:
Nitromethan-Kondensation mit Dialdehyden, VI; Nucleoside II.
Theophyllin-Nucleoside der 3-Amino-3-deoxy-β-D-glucose, -mannose und -galactose.
Chem. Ber. 1967, 100, 1833-1844.
29. F.W. Lichtenthaler, H. Leinert, T. Suami:
A Simple Synthesis of Streptamine and Actinamine.
Angew. Chem. 1967, 79, 239-240; Angew. Chem. Int. Ed. Engl. 1967, 6, 254.
28. F.W. Lichtenthaler, P. Emig:
NMR-Studies on Sugars and Cyclanols, III. On the Configuration of C-Methyl-branched Sugars and Cyclanols at the Branching Point.
Tetrahedron Lett. 1967, 577-582.
1966
27. F.W. Lichtenthaler, H. Leinert, H. K.Yahya:
Synthese verzweigter Nitro- und Amino-cyclanole.
Z. Naturforschg. 1966, 21b, 1004-1005.
26. F.W. Lichtenthaler, H. Zinke:
Synthese C-Methyl-verzweigter Uracil-Nucleoside.
Angew. Chem. 1966, 78, 774-775; Angew. Chem. Int. Ed. Engl. 1966, 5, 737.
25. F.W. Lichtenthaler:
Rezension von "R.W. Bailey: Oligosaccharides. A Comprehensive Account of all known Sugars of the Oligosaccharides Class of Compounds",
Pergamon Press, Oxford 1965.
Angew. Chem. 1966, 78, 651; Angew. Chem. Int. Ed. Engl. 1966, 5, 620.
24. T. Suami, F.W. Lichtenthaler, S. Ogawa:
Aminocyclitols, VIII. A Synthesis of Inosamines and Inosadiamines.
Bull. Chem. Soc. Jap. 1966, 39, 170-178.
23. F.W. Lichtenthaler, H. Leinert:
NMR-Studien an Zuckern und Cyclanolen, II. cis- Inosatriamin-(1,3,5).
Chem. Ber. 1966, 99, 903-907.
22. F.W. Lichtenthaler, H.P. Albrecht:
Nitromethan-Kondensation mit Dialdehyden, V; Nucleoside I. Hypoxanthin- und Uracil-Nucleoside der 3'-Nitro- und 3'-Amino-3'- desoxy-glucopyranose.
Chem. Ber. 1966, 99, 575-585.
1965
21. F.W. Lichtenthaler:
Rezension von R.D. Guthrie and J. Honeyman, "An Introduction to the Chemistry of Carbohydrates", Clarendon Press, Oxford 1964.
Angew. Chem. 1965, 77, 980; Angew. Chem. Int. Ed. Engl. 1965, 4, 1002.
20. T. Suami, F.W. Lichtenthaler, S. Ogawa:
Aminocyclitols, V. A New Synthesis of 2-Amino-1,3-cyclohexandiol.
Bull. Chem. Soc. Jap. 1965, 38, 754-757.
19. J. Yoshimura, F.W. Lichtenthaler:
NMR-Spektroskopische Ermittlung der Konfigurationen von Zuckern und Cyclanolen anhand ihrer Trimethylsilyläther.
Angew. Chem. 1965, 77, 740; Angew. Chem. Int. Ed. Engl. 1965, 4, 716.
18. F.W. Lichtenthaler, H.P. Albrecht, G. Olfermann, J. Yoshimura:
Synthese von 3'-Aminonucleosiden.
Angew. Chem. 1965, 77, 731; Angew. Chem. Int. Ed. Engl. 1965, 4, 706.
17. F.W. Lichtenthaler, H.K. Yahya:
Nitromethan-Kondensation mit Dialdehyden, IV. 4-Desoxy-4- nitro-Derivative der Sorbo- und Tagatopyranose.
Tetrahedron Lett. 1965, 1805-1811.
16. F.W. Lichtenthaler, H.P. Albrecht, G. Olfermann:
Cyclisierung von "Nucleosid-Dialdehyden" mit Nitromethan.
Angew. Chem. 1965, 77, 131; Angew. Chem. Int. Ed. Engl. 1965, 4, 147.
1964
15. M. Nakajima, A. Hasegawa, F.W. Lichtenthaler:
Zur Chemie des Benzolglykols, XII. Synthese von Desoxy- inosaminen.
Liebigs Ann. Chem. 1964, 680, 21-31.
14. F.W. Lichtenthaler:
Cyclisierung von Dialdehyden mit Nitromethan.
Angew. Chem. 1964, 76, 84-97; Angew. Chem. Int. Ed. Engl. 1964, 3, 211- 224.

1963
13. M. Nakajima, A. Hasegawa, F.W. Lichtenthaler:
Zur Chemie des Benzolglykols, XI. Synthese von Inosadiaminen.
Liebigs Ann. Chem. 1963, 669, 75-84.
12. F.W. Lichtenthaler:
Nitromethan-Kondensation mit Dialdehyden, III. Cyclisierung aromatischer Dialdehyde mit Nitromethan.
Tetrahedron Lett. 1963, 775-779.
11. F.W. Lichtenthaler:
NMR-Studien an Zuckern und Cyclanolen, I. Die Konfigurationsermittlung von Aminocyclohexanpolyolen durch Protonenresonanzspektroskopie.
Chem. Ber. 1963, 96, 2047-2051.
10. F.W. Lichtenthaler: Nitromethan-Kondensation mit Dialdehyden, II. Zur Synthese von myo-Inosit aus Glucose.
Angew. Chem. 1963, 75, 93; Angew. Chem. Int. Ed. Engl. 1963, 1, 662.
9. F.W. Lichtenthaler:
Nitromethan-Kondensation mit Dialdehyden, I. Synthese von 2- Amino-cyclohexandiolen-(1,3).
Chem. Ber. 1963, 96, 845-853.
1962
8. F.W. Lichtenthaler:
Melvin Calvin: Nobelpreis für Chemie 1961.
Ruperto Carola (Heidelberg) 1962, 31, 24- 26.
7. F.W. Lichtenthaler:
Kondensation von Glutardialdehyd mit Nitromethan.
Angew. Chem. 1962, 74, 504.
6. F.W. Lichtenthaler, F. Cramer:
Zur Chemie der "energiereichen Phosphate", XVII. Über die Reaktivität von Enolphosphaten.
Chem. Ber. 1962, 95, 1971-1982.
1961
5. F.W. Lichtenthaler:
Nitromethan-Kondensation von Pentandial-1,5.
Angew. Chem. 1961, 73, 654.
4. F.W. Lichtenthaler:
Konfiguration der bei Cyclisierung von 6-Nitro-D-glucose gebildeten Desoxy-nitro-inosite und ihre Isomerisierungen mit Alkali.
Chem. Ber. 1961, 94, 3071-3085.
3. F.W. Lichtenthaler, H.O.L.Fischer:
Cyclizations of Dialdehydes with Nitromethane, VII. Preparation of neo-Inosadiamine-1.4.
J. Am. Chem. Soc. 1961, 83, 2005-2012.
2. F.W. Lichtenthaler:
Chemistry and Properties of Enol Phosphates.
Chem. Rev. 1961, 61, 607-649.
Based, in part, on: F.W. Lichtenthaler, "Über die Reaktivität von Enolphosphaten", Dissertation, Univ. Heidelberg, 1959.
1958
1. F. Cramer, K. Pawelzik, F.W. Lichtenthaler:
Die Reaktion von Imidoestern mit Säuren (Pinner-Spaltung).
Chem. Ber. 1958, 91, 1555-1562.
Based, in part, on: F. W. Lichtenthaler, "Zur Pinner-Reaktion mit Phosphorsäuren", Diplomarbeit, Univ. Heidelberg, 1957.


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