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asymmetric synthesis
(redirected from Stereoselective synthesis)

   Also found in: Wikipedia 0.03 sec.

asymmetric synthesis

Chemical reaction by which unequal amounts of two product isomers are formed. It is normally not possible to synthesize from materials that do not have optical activity (i.e., are not chiral) one stereoisomer of a chiral compound without the other, but use of a chiral auxiliary, such as an enzyme or other catalyst, a solvent, or an intermediate, can force the reaction to produce predominantly or only one isomer. Asymmetric syntheses are often called stereoselective; if one product forms exclusively, it is stereospecific.


asymmetric synthesis [¦ā·sə¦me·trik ′sin·thə·səs]
(organic chemistry)
Chemical synthesis of a pure enantiomer, or of an enantiomorphic mixture in which one enantiomer predominates, without the use of resolution.


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00 Paperback QD262 Carreira (organic chemistry, ETH-Zurich, Switzerland) and Kvaerno (process chemist, Lundbeck, Copenhagen) have written this textbook on stereoselective synthesis for students and researchers in the field of synthetic organic chemistry who must deal with drug and natural product syntheses on a daily basis.
His research interests include the stereoselective synthesis of natural products, new methods in synthetic organic chemistry, and computational organometallic chemistry in organic synthesis.
An industrial perspective is given on the stereoselective synthesis of drugs, aspects of chirality in natural products drug discovery are examined, and biotransformation methods for preparing chiral drugs and drug intermediates are presented.
 
 
 
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