Prochirality

From Wikipedia, the free encyclopedia
Jump to: navigation, search
An sp2-hybridized carbon atom, with re and si faces.

In stereochemistry, prochiral molecules are those that can be converted from achiral to chiral in a single step.[1][2] An achiral species which can be converted to a chiral in two steps is called proprochiral.[2]

If two identical substituents are attached to a sp3-hybridized atom, the descriptors pro-R and pro-S are used to distinguish between the two. Promoting the pro-R substituent to higher priority than the other identical substituent results in an R chirality center at the original sp3-hybridized atom, and analogously for the pro-S substituent.

A trigonal planar sp2-hybridized atom can be converted to a chiral center when a substituent is added to the re or si face of the molecule. A face is labeled re if, when looking at that face, the substituents at the trigonal atom are arranged in decreasing Cahn-Ingold-Prelog priority order in a clockwise order, and si if the priorities decrease in counter-clockwise order; but the designation of the resulting chiral center as S or R depends on the priority of the incoming group.

References[edit]

  1. ^ John McMurry. Organic Chemistry (6ed ed.). Brooks/Cole. pp. 301–303. 
  2. ^ a b IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version:  (2006–) "prochirality".