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, this book presents a
detailed analysis of the factors that govern stereoselectivity in
organic reactions.
After an explanation of the basic physical-organic principles
governing stereoselective reactions, the authors provide a
detailed, annotated glossary of stereochemical terms. A chapter on
"Practical Aspects of Asymmetric Synthesis" provides a critical
overview of the most common methods for the preparation of
enantiomerically pure compounds, techniques for analysis of
stereoisomers using chromatographic, spectroscopic, and chiroptical
methods.
The authors then present an overview of the most important
methods in contemporary asymmetric synthesis organized by reaction
type. Thus, there are four chapters on carbon-carbon bond forming
reactions, one chapter on reductions, and one on oxidations
(carbon-oxygen and carbon-nitrogen bond forming reactions). This
organization allows the reader to compare the leading methods for
asymmetric synthesis in an appropriate context.
A highlight of the book is the presentation and discussion of
transition states at the current level of understanding, for
important reaction types. In addition, extensive tables of examples
are used to give the reader an appreciation for the scope of each
reaction. Finally, leading references are provided to natural
product synthesis that has been accomplished using a given reaction
as a key step.
Authoritative glossary to aid understanding of stereochemical
terminologyExplanations of the key factors influencing
stereoselectivity with numerous examples, organized by reaction
typeA handy reference guide to the literature of asymmetric
synthesis for practitioners in the field
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