z-logo
open-access-imgOpen Access
Mirror, mirror on the wall ... stereochemistry in therapeutics.
Author(s) -
Dan M. Roden
Publication year - 1994
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/01.cir.89.5.2451
Subject(s) - stereochemistry , medicine , chemistry
Stereoisomers are molecules that have the same structural formulas but differ in the orientation of their individual atoms in space.1-3A special form of isomerism occurs when an individual atom, or chiral center (usually a carbon), has four different substituents arranged in a tetrahedral fashion. In this case, two mirrorimage orientations, called enantiomers, of these substituents around the chiral center are possible. Enantiomers are identified by the way in which they rotate polarized light: the terms dextrorotary (dor [+]-enantiomer) and levorotary (1or [-1-enantiomer) are used, as is an alternate (and not interchangeable) system in which enantiomers are more rigorously termedRand S-.'A number of

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom