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Alexandre Alexakis - Copper-Catalyzed Asymmetric Synthesis

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Alexandre Alexakis Copper-Catalyzed Asymmetric Synthesis

Copper-Catalyzed Asymmetric Synthesis: summary, description and annotation

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This book reflects the increasing interest among the chemical synthetic community in the area of asymmetric copper-catalyzed reactions, and introduces readers to the latest, most significant developments in the field.
The contents are organized according to reaction type and cover mechanistic and spectroscopic aspects as well as applications in the synthesis of natural products. A whole chapter is devoted to understanding how primary organometallics interact with copper to provide selective catalysts for allylic substitution and conjugate addition, both of which are treated in separate chapters. Another is devoted to the variety of substrates and experimental protocols, while an entire chapter covers the use on non-carbon nucleophiles. Other chapters deal with less-known reactions, such as carbometallation or the additions to imines and related systems, while the more established reactions cyclopropanation and aziridination as well as the use of copper (II) Lewis acids are warranted their own special chapters. Two further chapters concern the processes involved, as determined by mechanistic studies. Finally, a whole chapter is devoted to the synthetic applications.
This is essential reading for researchers at academic institutions and professionals at pharmaceutical or agrochemical companies.

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Related Titles Cornils B Herrmann WA Wong C-H Zanthoff H-W eds - photo 1

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The Editors

Prof. Dr. Alexandre Alexakis

University of Geneva

Dept. of Organic Chemistry

Postfach 30

1211 Genve 4

Switzerland

Prof. Dr. Norbert Krause

University Dortmund

Organic Chemistry II

Otto-Hahn-Str. 6

44227 Dortmund

Germany

Prof. Dr. Simon Woodward

University Of Nottingham

School of Chemistry

University Park

Nottingham NG7 2RD

United Kingdom

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 .

2014 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: 978-3-527-33204-5

ePDF ISBN: 978-3-527-66460-3

ePub ISBN: 978-3-527-66459-7

mobi ISBN: 978-3-527-66458-0

oBook ISBN: 978-3-527-66457-3

List of Contributors

Shinya Adachi
North Dakota State University
Department of Chemistry and Biochemistry
1231 Albrecht Boulevard
Fargo
ND 58108
USA
Alexandre Alexakis
University of Geneva
Department of Organic Chemistry
Postfach 30
1211 Genve 4
Switzerland
Olivier Basl
Ecole Nationale Suprieure de Chimie de Rennes CNRS
UMR 6226
11 Alle de
Beaulieu
CS 50837
35708 Rennes Cedex 7
France
Jeffrey Buter
Stratingh Institute for Chemistry
Department of Bio-Organic Chemistry
Nijenborgh 7
9747 AG Groningen
The Netherlands
Beatriz C. Calvo
Stratingh Institute for Chemistry
Department of Bio-Organic Chemistry
Nijenborgh 7
9747 AG Groningen
The Netherlands
Andr B. Charette
Universit de Montral
Centre in Green Chemistry and Catalysis
Dpartement de Chimie
Station Downtown
Montral
Qubec
H3C 3J7
Canada
Christophe Crvisy
Ecole Nationale Suprieure de Chimie de Rennes CNRS
UMR 6226
11 Alle de
Beaulieu
CS 50837
35708 Rennes Cedex 7
France
Audrey Denicourt-Nowicki
Ecole Nationale Suprieure de Chimie de Rennes CNRS
UMR 6226
11 Alle de
Beaulieu
CS 50837
35708 Rennes Cedex 7
France
Dorian Didier
Technion-Israel Institute of Technology
Schulich Faculty of Chemistry and the Lise Meitner-Minerva Center for Computational Quantum Chemistry
Technion City
Haifa 32000
Israel
Ruth M. Gschwind
University of Regensburg
Institute of Organic Chemistry
Universittsstrasse 31
93040 Regensburg
Germany
Hajime Ito
Hokkaido University
Division of Chemical Process Engineering
Faculty of Enginnering
Sapporo 060-8628
Japan
Carina Koch
University of Regensburg
Institute of Organic Chemistry
Universittsstrasse 31
93040 Regensburg
Germany
Norbert Krause
University Dortmund
Organic Chemistry II
Otto-Hahn-Str. 6
44227 Dortmund
Germany
and
University of Geneva
Department of Organic Chemistry
Postfach 30
1211 Geneva
Switzerland
Per-Fredrik Larsson
Akzo Nobel Functional Chemicals AB
Uddevallavgen 17
Stenungsund SE-444 85
Sweden
and
University of Gothenburg
Department of Chemistry and Molecular Biology
Kemivgen 10
SE-412 96 Gothenburg
Sweden
Hlne Lebel
Universit de Montral
Centre in Green Chemistry and Catalysis
Dpartement de Chimie
Station Downtown
Montral
Qubec
H3C 3J7
Canada
Hailing Li
University of Geneva
Department of Organic Chemistry
quai Ernest Ansermet 30
1211, Geneva 4,
Switzerland
Bruce H. Lipshutz
University of California
Department of Chemistry and Biochemistry
Santa Barbara
CA 93106
USA
Ilan Marek
Technion-Israel Institute of Technology
Schulich Faculty of Chemistry and the Lise Meitner-Minerva Center for Computational Quantum Chemistry
Technion City
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