One-pot deacylation-debromination reactions involving the transesterificati
on of the initial chiral beta-bromo-beta-hydroxy thioimide aldol adducts an
d subsequent Al-Hg mediated reductive cleavage of the C-Br bond allow for a
facile synthesis of enantiopure beta-hydroxy esters. (C) 2000 Published by
Elsevier Science Ltd.