Glycoscience: Chemistry and Chemical Biology I–IIIBertram O. Fraser-Reid, Kuniaki Tatsuta, Joachim Thiem Springer Science & Business Media, 2002 M01 1 - 2872 pages Glycostructures play a highly diverse and crucial role in a myriad of organisms and important systems in biology, physiology, medicine, bioengineering and technology. Only in recent years have the tools been developed to partly understand the highly complex functions and the chemistry behind them, but many facts still remain undiscovered. "All roads lead to carbohydrates ... we cannot do without them." (K.C. Nicolaou). Presently the field is experiencing a "quantum jump". Therefore the editors have drawn together in this three volume set plus an accompanying CD-ROM, the complete and up-to-date information on glycostructures, their chemistry and chemical biology, and present them in the form of a comprehensive and strictly systematic survey. The texts are furnished by 2.670 figures, chemical structures and reaction schemes (including more than 12.000 individual chemical reactions), and more than 9.000 references. |
Contents
T Bruce Grindley | 4 |
5 | 5 |
Chapter 8 | 8 |
4 | 29 |
Properties of Carbohydrates | 54 |
3 | 64 |
5 | 70 |
General Occurrence of Carbohydrates | 76 |
Deoxygenation | 232 |
2 | 238 |
4 | 246 |
51 | 248 |
Heteroatom Exchange | 253 |
References | 362 |
Oligosaccharides | 490 |
Abbreviations | 627 |
Occurrence of DFructose in Polysaccharides | 88 |
Occurrence of Sugar Acids | 102 |
29 | 111 |
119 | |
3 | 131 |
7 | 138 |
OCarbonyl Compounds | 146 |
127 | 151 |
5 | 157 |
2 | 164 |
6 | 169 |
Deoxygenation | 232 |
2 | 238 |
4 | 255 |
5 | 275 |
4 | 305 |
References | 189 |
Volume II | 877 |
from Monosaccharides | 1175 |
Throughout this chapter unless otherwise stated B Bacyl Bacyl and B | 1195 |
Summary | 1708 |
References | 1751 |
References | 1770 |
Glycolipids | 2083 |
Glycoproteins | 2255 |
References | 2283 |
Synthesis and Applications of Biologically Relevant | 2307 |
Glycopeptides as Antibiotics and Other Drug Targets | 2323 |
8 | 2349 |
Introduction | 2381 |
Glycomimetics | 2533 |
C | 2625 |
2847 | |
Other editions - View all
Glycoscience: Chemistry and Chemical Biology Bertram O. Fraser-Reid,Kuniaki Tatsuta,Joachim Thiem No preview available - 2001 |
Common terms and phrases
acetate acid AcO OAC Adv Carbohydr Chem AIBN alcohol aldehyde aldol anomeric effect B(acyl BnO BnO BnO BnO OBn C-glycosides Carbohydr Chem Biochem Carbohydr Res carbon carboxylic catalyst CH₂ CH3 CH3 Chem Lett Chem Soc Chem Chem Soc Perkin chemistry chloride compound conformation cyclic D-glucose deoxygenation derivatives disaccharide double bond epoxide ester ethers formation Fraser-Reid give glycals glycosides glycosyl glycosyl donors H₂C CH3 H₂O hemiacetal hydrogen hydroxy hydroxy group intermediate lactone leaving group m-CPBA method methyl mixture monosaccharides nucleophile nucleosides OAC AcO OAC OAC OBn BnO OBn OBn OH HO OH OH OH OH oligosaccharides OMe OMe oxidation polysaccharides prepared protecting groups pyranose pyridine reaction reactive reagent rearrangement reduction regioselective ring saccharides Scheme 15 shown in Scheme Soc Chem Commun Soc Perkin Trans sodium solvent stereoselectivity substitution sugars synthesis TBDMS Tetrahedron Lett tetrahydrofuran thioglycosides tion unsaturated yield ÎÍ