A general synthesis of C-4-substituted dihydropyridines is described.
The route exploits a standard Hantzsch ester synthesis followed by nuc
leophilic substitution of a halide with, for example, triethylphosphit
e. The resulting compounds could have interesting biological propertie
s or may find use as haptens for preparing catalytic antibodies for hy
dride transfer reactions. Copyright (C) 1996 Published by Elsevier Sci
ence Ltd