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Asymmetric synthesis

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Published by Blackie Academic in London .
Written in English


Book details:

Edition Notes

Statementedited by R.A. Aitken and S. N. Kilenyi.
ContributionsAitken, R. A., Kilenyi, S. N.
The Physical Object
Pagination256p.
Number of Pages256
ID Numbers
Open LibraryOL14966494M
ISBN 100216927978
OCLC/WorldCa24718364

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Since this important work was first published in , the field of catalytic asymmetric synthesis has grown explosively, spawning effective new methods for obtaining enantiomerically pure compounds on a large scale and stimulating new applications in diverse fields—from medicine to materials science. Contributors; If one could prepare 2-hydroxypropanenitrile from ethanal and hydrogen cyanide in the absence of any chiral reagent and produce an excess of one enantiomer over the other, this would constitute an absolute asymmetric synthesis - that is, creation of preferential chirality (optical activity) in a symmetrical environment from symmetrical reagents. The book is organized into five chapters, each with an introductory preface. Starting from the key concepts of asymmetric synthesis diastereoselective methods, asymmetric catalysis) the Focus then shifts to its application to the synthesis natural products and industrial vanbuskirkphotos.com: Mathias Christmann. Mar 18,  · Here, all aspects of the topic are presented in a compact manner. The book is clearly structured, and divided into two sections -- asymmetric synthesis of heterocycles containing only one nitrogen and that of those with more than one nitrogen as a heteroatom -- such that the necessary information may be found at a glance.

Asymmetric Synthesis. Book • Edited by: James D. Morrison. Browse book content. About the book. Search in this book. Search in this book. Browse content Table of contents. Select all Front Matter. 4 - Asymmetric Hydrosilylation and Hydrocarbonylation. . Asymmetric synthesis is one of the most important areas of research and development in synthetic organic chemistry, and has wide-ranging industrial applications. This introduction to the subject covers chirality, nomenclature and analytical methods of resolution. The main body of the text describes the principal methods available to the organic chemist wishing to synthesize chiral compounds. This book focuses on different techniques of asymmetric synthesis of important compounds, such as drugs and natural products. It gives insightful information on recent asymmetric synthesis by Inorganic, Organic and Enzymatic combinations. It also emphasizes chiral compounds and design of new catalys. Asymmetric synthesis is an integral part of synthetic organic chemistry. Some of the reactions in this book were known prior to , while several new ones, particularly catalytic asymmetric reactions, have been discovered in the recent years. The impact of this new class of reactions has been imp.

Catalytic Asymmetric Synthesis, Third Edition addresses these rapid changes through contributions from highly recognized world leaders in the field. This book is an excellent state-of-the-art compilation of catalytic asymmetric chemistry and should be included in any chemistry reference vanbuskirkphotos.com: $ Cite as: vanbuskirkphotos.comdium of Chemical Terminology, 2nd ed. (the "Gold Book"). Compiled by A. D. McNaught and A. Wilkinson. Blackwell Scientific Publications, Oxford. Catalytic Asymmetric Synthesis, Third Edition addresses these rapid changes through contributions from highly recognized world leaders in the field. This seminal text presents detailed accounts of the most important catalytic asymmetric reactions known today, and discusses recent advances and essential information on the initial development of Author: Iwao Ojima. The world is chiral. Most of the molecules in it are chiral, and asymmetric synthesis is an important means by which enantiopure chiral molecules may be obtained for study and sale. Using examples from the literature of asymmetric synthesis (more than references), the aim of this book is to present a detailed analysis of the factors that govern stereoselectivity in organic reactions.5/5(1).