Classics in Stereoselective Synthesis

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Edition: 1st
Format: Paperback
Pub. Date: 2009-02-09
Publisher(s): Wiley-VCH
List Price: $112.37

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Summary

Providing an excellent compilation of the most important and useful methods of modern stereoselective synthesis, this book features illustrative examples of drug and natural product syntheses, resulting in a rich source of stimulating ideas for the efficient use of asymmetric reactions in the users' own synthesis. The authors adopt a novel approach in not attempting to present this rapidly developing area in its entirety, but to distill the truly groundbreaking reactions that should be in the repertoire of every synthetic organic chemist.

Author Biography

Professor Carreira obtained his Ph.D. degree in 1990 from Harvard University and became Assistant Professor at the same faculty in 1992. After becoming full professor in 1997 he moved to ETH Z++rich in 1998. He is recipient of many awards among them the Nobel Laureate Signature Award and the ACS Award in Pure Chemistry. His research focuses on asymmetric synthesis of natural products.

Dr. Lisbet Kvaerno received her PhD in 2004 and worked as a Postdoc at the ETH Zuerich, Switzerland in the group of Erick M. Carreira. After a second postdoctoral stay at Harvard in he group of David A. Evans she moved to Germany where she is currently an Independent Junior Group Leader at the Max Planck Institute of Coal Research. Research in her group is focused on organic synthesis and the discovery of new reaction methodology, in particular stereoselective and catalytic asymmetric reactions.

Table of Contents

Macrocyclic Stereocontrol Carbony
l Addition Reactions alpha-Functionalization of Enolates Aldol Reactions Allylations of C=O Bonds Chiral
Acetals Alkene
Hydroboration Reductions of Olefins
Oxidations of Olefins
Amino Acids Additions to C=N Bonds
Conjugate Additions Chiral Carbanions
Metal-Catalyzed Allylations
Cyclopropanations and CH-Insertion
Reactions Sigmatropic Rearrangements
Diels-Alder and Hetero-Diels-Alder
Reactions [3+2]- and [2+2]-Cycloaddition Reactions
Table of Contents provided by Publisher. All Rights Reserved.

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