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Clay S. Bennett - Selective Glycosylations: Synthetic Methods and Catalysts

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Clay S. Bennett Selective Glycosylations: Synthetic Methods and Catalysts
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    Selective Glycosylations: Synthetic Methods and Catalysts
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Selective Glycosylations: Synthetic Methods and Catalysts: summary, description and annotation

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A comprehensive summary of novel approaches to the stereoselective construction of glycosidic linkages, covering modern glycosylation methods and their use and application in natural product synthesis and drug discovery.
Clearly divided into five sections, the first describes recent advances in classical methodologies in carbohydrate chemistry, while the second goes on to deal with newer chemistries developed to control selectivity in glycosylation reactions. Section three is devoted to selective glycosylation reactions that rely on the use of catalytic promoters. Section four describes modern approaches for controlling regioselectivity in carbohydrate synthesis. The final section focuses on new developments in the construction of unusual sugars and is rounded off by a presentation of modern procedures for the construction of glycosylated natural products.
By providing the latest advances in glycosylation as well as information on mechanistic aspects of the reaction, this is an invaluable reference for both specialists and beginners in this booming interdisciplinary field that includes carbohydrate chemistry, organic synthesis, catalysis, and biochemistry.

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Editor Prof Clay S Bennett Tufts University Department of Chemistry 62 - photo 1

Editor

Prof. Clay S. Bennett

Tufts University

Department of Chemistry

62 Talbot Ave.

Medford, MA 02155

United States

Cover

The cover image was kindly provided by the Editor

All books published by Wiley-VCH are carefully produced. Nevertheless, authors, editors, and publisher do not warrant the information contained in these books, including this book, to be free of errors. Readers are advised to keep in mind that statements, data, illustrations, procedural details or other items may inadvertently be inaccurate.

Library of Congress Card No.: applied for

British Library Cataloguing-in-Publication Data

A catalogue record for this book is available from the British Library.

Bibliographic information published by the Deutsche Nationalbibliothek

The Deutsche Nationalbibliothek lists this publication in the Deutsche Nationalbibliografie; detailed bibliographic data are available on the Internet at http://dnb.d-nb.de.

2017 Wiley-VCH Verlag GmbH & Co. KGaA, Boschstr. 12, 69469 Weinheim, Germany

All rights reserved (including those of translation into other languages). No part of this book may be reproduced in any form by photoprinting, microfilm, or any other means nor transmitted or translated into a machine language without written permission from the publishers. Registered names, trademarks, etc. used in this book, even when not specifically marked as such, are not to be considered unprotected by law.

Print ISBN: 978-3-527-33987-7

ePDF ISBN: 978-3-527-69622-2

ePub ISBN: 978-3-527-69624-6

Mobi ISBN: 978-3-527-69625-3

oBook ISBN: 978-3-527-69623-9

Cover Design Schulz Grafik-Design, Fugnheim, Germany

List of Contributors
  1. Mithila D. Bandara
  2. University of Missouri - St. Louis
  3. Department of Chemistry and Biochemistry
  4. One University Blvd.
  5. St. Louis, MO 63121
  6. USA
  1. David Benito-Alifonso
  2. University of Bristol
  3. School of Chemistry
  4. Cantock's Close
  5. Bristol BS8 1TS
  6. UK
  1. Clay S. Bennett
  2. Tufts University
  3. Department of Chemistry
  4. 62 Talbot Ave.
  5. Medford, MA 02155
  6. USA
  1. Luis Boh
  2. Institut de Chimie des Substances Naturelles
  3. CNRS-ICSN UPR2301
  4. Universit Paris-Sud
  5. Avenue de la Terrasse
  6. 91198 Gif-sur-Yvette
  7. France
  1. Robin Brabham
  2. York Structural Biology Laboratory
  3. Department of Chemistry
  4. University of York
  5. Heslington, York
  6. YO10 5DD
  7. UK
  1. Jeroen D.C. Code
  2. Leiden University
  3. Leiden Institute of Chemistry
  4. PO Box 9502
  5. 2300 RA Leiden
  6. The Netherlands
  1. David Crich
  2. Wayne State University
  3. Department of Chemistry
  4. 5101 Cass Ave.
  5. Detroit, MI 48202
  6. USA
  1. Alexei V. Demchenko
  2. University of Missouri - St. Louis
  3. Department of Chemistry and Biochemistry
  4. One University Blvd.
  5. St. Louis, MO 63121
  6. USA
  1. Alisa E. R. Fairweather
  2. University of Iowa
  3. Department of Chemistry
  4. E331 Chemistry Building
  5. Iowa City, IA 52245
  6. USA
  1. Martin A. Fascione
  2. York Structural Biology Laboratory
  3. Department of Chemistry
  4. University of York
  5. Heslington, York
  6. YO10 5DD
  7. UK
  1. M. Carmen Galan
  2. University of Bristol
  3. School of Chemistry
  4. Cantock's Close
  5. Bristol BS8 1TS
  6. UK
  1. Carola Gallo-Rodriguez
  2. Universidad de Buenos Aires
  3. CIHIDECAR Departamento de Qumica Orgnica
  4. Ciudad Universitaria, Pabelln II
  5. 1428 Buenos Aires
  6. Argentina
  1. Bas Hagen
  2. Leiden University
  3. Leiden Institute of Chemistry
  4. PO Box 9502
  5. 2300 RA Leiden
  6. The Netherlands
  1. Thomas Hansen
  2. Leiden University
  3. Leiden Institute of Chemistry
  4. PO Box 9502
  5. 2300 RA Leiden
  6. The Netherlands
  1. Kim Le Mai Hoang
  2. Nanyang Technological University
  3. Division of Chemistry and Biological Chemistry
  4. School of Physical and Mathematical Sciences
  5. SPMS-CBC-02-01
  6. 21 Nanyang Link, 637371
  7. Singapore
  1. Akihiro Ishiwata
  2. RIKEN
  3. Synthetic Cellular Chemistry Laboratory
  4. 2-1 Hirosawa Wako
  5. Saitama 351-0198
  6. Japan
  1. Yukishige Ito
  2. RIKEN
  3. Synthetic Cellular Chemistry Laboratory
  4. 2-1 Hirosawa Wako
  5. Saitama 351-0198
  6. Japan
  1. Gustavo A. Kashiwagi
  2. Universidad de Buenos Aires
  3. CIHIDECAR Departamento de Qumica Orgnica
  4. Ciudad Universitaria, Pabelln II
  5. 1428 Buenos Aires
  6. Argentina
  1. Suvarn S. Kulkarni
  2. Indian Institute of Technology Bombay
  3. Department of Chemistry
  4. Powai
  5. Mumbai 400076
  6. India
  1. Wei-Lin Leng
  2. Nanyang Technological University
  3. Division of Chemistry and Biological Chemistry
  4. School of Physical and Mathematical Sciences
  5. SPMS-CBC-02-01
  6. 21 Nanyang Link, 637371
  7. Singapore
  1. Yu-Hsuan Lih
  2. Genomics Research Center, Academia Sinica
  3. 128 Academia Road, Section 2, Nankang
  4. Taipei 115
  5. Taiwan
  1. Xue-Wei Liu
  2. Nanyang Technological University
  3. Division of Chemistry and Biological Chemistry
  4. School of Physical and Mathematical Sciences
  5. SPMS-CBC-02-01
  6. 21 Nanyang Link, 637371
  7. Singapore
  1. Ravi S. Loka
  2. University of Iowa
  3. Department of Chemistry
  4. E331 Chemistry Building
  5. Iowa City, IA 52245
  6. USA
  1. Gijs van der Marel
  2. Leiden University
  3. Leiden Institute of Chemistry
  4. PO Box 9502
  5. 2300 RA Leiden
  6. The Netherlands
  1. KwoK-Kong Tony Mong
  2. National Chiao Tung University
  3. Applied Chemistry Department
  4. 1001 Ta Hsueh Road
  5. Hsinchu 300
  6. Taiwan ROC
  1. Hien M. Nguyen
  2. University of Iowa
  3. Department of Chemistry
  4. E331 Chemistry Building
  5. Iowa City, IA 52245
  6. USA
  1. Pham Be Nhi
  2. National Chiao Tung University
  3. Applied Chemistry Department
  4. 1001 Ta Hsueh Road
  5. Hsinchu 300
  6. Taiwan ROC
  1. Toshiki Nokami
  2. Tottori University
  3. Department of Chemistry and Biotechnology
  4. 4-101 Koyama-Minami
  5. Tottori city
  6. 680-8552 Tottori
  7. Japan
  1. George A. O'Doherty
  2. Northeastern University
  3. Department of Chemistry and Chemical Biology
  4. 360 Huntington Ave.
  5. Boston, MA 02115
  6. USA
  1. Justin Ragains
  2. Louisiana State University
  3. Department of Chemistry
  4. 232 Choppin Hall
  5. Baton Rouge, LA 70803
  6. USA
  1. Pei Shi
  2. Corden Pharma
  3. 1-B Gill Street
  4. Woburn, MA 01801
  5. USA
  1. Eric T. Sletten
  2. University of Iowa
  3. Department of Chemistry
  4. E331 Chemistry Building
  5. Iowa City, IA 52245
  6. USA
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