
Organic Synthesis with Carbohydrates
Wiley (Publisher)
Published on 28. January 2008
Software
Other digital
348 pages
978-0-470-76032-1 (ISBN)
Description
Carbohydrates offer a ready source of enantiomerically pure starting materials. They have been used for the imaginative synthesis of a wide range of compounds, and have been found to be effective chiral auxiliaries which enable the introduction of a range of functionalities in a highly enantioselective manner. In a subject dominated by volumes at research and professional level, this book provides a broad understanding of the use of carbohydrates in organic synthesis, at postgraduate student level. Emphasis is placed on retrosynthetic analysis, with discussion of why a particular synthetic route has been chosen, and mechanistic explanations are provided for key and novel reactions. Wherever possible, the authors highlight points of general significance to organic synthesis. Selected experimental conditions and reaction details are incorporated to ensure that information can be utilised in research. The book is extensively referenced and so provides a convenient point of entry to the primary literature.
More details
Language
English
Place of publication
Hoboken
United Kingdom
Publishing group
John Wiley and Sons Ltd
Target group
Professional and scholarly
Dimensions
Height: 239 mm
Width: 165 mm
Thickness: 26 mm
Weight
648 gr
ISBN-13
978-0-470-76032-1 (9780470760321)
Copyright in bibliographic data and cover images is held by Nielsen Book Services Limited or by the publishers or by their respective licensors: all rights reserved.
Schweitzer Classification
Other editions
Additional editions

Geert-Jan Boons | Karl J. Hale
Organic Synthesis with Carbohydrates
E-Book
05/2008
Wiley-Blackwell
€105.99
Available for download
Persons
Author
Complex Carbohydrates Research Center, Athens, Georgia, USA
Department of Chemistry, University College, London, UK
Content
Part A: Structure and Synthesis of Saccharides and Glycoproteins. 1 Mono- and oligosaccharides: structure, configuration and conformation. 2 Protecting groups. 3 Functionalised saccharides. 4 Oligosaccharide synthesis. 5 The chemistry of O- and N-linked glycopeptides. Part B: Natural Product Synthesis from Monosaccharides. 6 (-)-Echinosporin. 7 (+)Zaragozic acid C. 8 (+)-Neocarzinostatin. 9 (+)-Castanospermine. 10 (-)-Silphiperfolene. 11 (-)-Allosamizoline. 12 (-)-Reiswigin A. 13 (-)-Octalactin A. 14 (-)-ACRL toxin I. 15 (+)-Gasbosine E. 16 (-)-Augustamine and (-)-amabiline. 17 (-)-FK506. 18 (3S, 5S)-5-Hydroxypiperazic acid. References. Index.