M. Shibasaki et Em. Vogl, The palladium-catalysed arylation and vinylation of alkenes - enantioselective fashion, J ORGMET CH, 576(1-2), 1999, pp. 1-15
The enantioselective Heck reaction is a powerful method for the synthesis o
f both tertiary and quaternary chiral carbon centres, with enantiomeric exc
esses (ees) often around 80% and in some cases much higher. A variety of ca
rbocyclic and heterocyclic systems can be constructed or modified including
spirocyclic systems. Although problems of regioselectivity with respect to
the product alkene continue to limit the scope of the reaction somewhat, t
here are indications that these may be surmountable and that a new generati
on of ligands and a refined methodology, may improve both enantio- and regi
ocontrol. All the relevant literature is discussed. (C) 1999 Elsevier Scien
ce S.A. All rights reserved.