Catalysis in Asymmetric Synthesis

Asymmetric synthesis has become a major aspect of modern organic chemistry. The importance of stereochemical purity in pharmaceutical products has been one driving force in the quest for improved control over the stereochemical outcome of organic reactions. Asymmetric catalysis is an important aspect of asymmetric synthesis, and one that has seen tremendous activity over the past decade. This book is planned from the point of view of the synthetic organic chemist, i.e. by transformation rather than on the basis of the organometallic chemistry. The emphasis is on non–enzymatic methods of asymmetric catalysis, although key references to enzyme–catalysed reactions have been incorporated where appropriate.
The book is extensively referenced and so provides a convenient point of entry to the primary literature.

Spis treści:
Introduction.
Reduction of alkenes.
Reduction of ketones and imines.
Epoxidation of alkenes.
Further oxidation reactions.
Nucleophilic addition to carbonyl compounds.
The aldol and related reactions.
The Diels–Alder reaction and related transformations.
Catalytic reactions involving metal carbenoids.
Catalytic carbon–carbon bond–forming reactions.
Conjugate addition reactions.
Further catalytic reactions.
Index

Okładka tylna:
Asymmetric synthesis has become a major aspect of modern organic chemistry. The importance of stereochemical purity in pharmaceutical products has been one driving force in the quest for improved control over the stereochemical outcome of organic reactions. Asymmetric catalysis is an important aspect of asymmetric synthesis, and one that has seen tremendous activity over the past decade. This book is planned from the point of view of the synthetic organic chemist, i.e. by transformation rather than on the basis of the organometallic chemistry. The emphasis is on non–enzymatic methods of asymmetric catalysis, alt hough key references to enzyme–catalysed reactions have been incorporated where appropriate.
The book is extensively referenced and so provides a convenient point of entry to the primary literature.