Handbook of Chemical Glycosylation
Advances in Stereoselectivity and Therapeutic Relevance

1. Edition February 2008
XXII, 502 Pages, Hardcover
492 Pictures
14 tables
Handbook/Reference Book
Short Description
Since glycosidic linkage is one of the major challenges in carbohydrate chemistry, this book on recent developments fulfils a great need in covering the chemistry necessary to synthesize exact copies of these structures.
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Since carbohydrate oligomers are still a challenge in synthetic chemistry, this book on recent developments fulfils a great need. Covering the chemistry necessary to synthesize exact copies of these structures, top authors from all around the world comprehensively deal with synthesis from anomeric halides, from miscellaneous glycosyl donors, and by indirect and special methods, as well as 1-oxygen-and 1-sulfur-substituted derivatives. They demonstrate the best approach for the stereoselective formation of the intermonomeric bond, making this essential reading for every biochemist working in biosynthesis, the exploration of biopathways and vaccines.
GLYCOSIDE SYNTHESIS FROM ANOMERIC HALIDES
Glycosyl Fluorides
Glycosyl Chlorides, Bromides, and Iodides
GLYCOSIDE SYNTHESIS FROM 1-OXYGEN-SUBSTITUTED GLYCOSYL DONORS
Hemiacetals and O-Acyl/Carbonyl Derivatives
Glycosyl Imidates
Anomeric Transglycosylation
Phosphites, Phosphates, and Other O--P Derivatives
GLYCOSIDE SYNTHESIS FROM 1-SULFUR/SELENIUM-SUBSTITUTED DERIVATIVES
Thioalkyl and Thioaryl Glycosides
Sulfoxides, Sulfimides, and Sulfones
Xanthates, Thioimidates, and Other Thio Derivatives
Selenoglycosides
OTHER METHODS FOR GLYCOSIDE SYNTHESIS
Orthoesters and Related Derivatives
Dehydro and Anhydro Derivatives
Miscellaneous Glycosyl Donors
Indirect and Special Methods