In order to evaluate the biological properties of new alpha-aminophosp
honic acids 4a-g bearing a pyrrolic or thiophenic moiety, their synthe
sis via the corresponding esters 3a-g is carried out by two methods. T
he standard procedure leading to alpha-aminophosphonic esters 3 in goo
d yields, requires heating of the neat reactants for several days. The
sonochemical activation improves substantially the rate of formation
of 3 and promotes the yields of the reaction. The rate enhancement for
this homogeneous sonochemical reaction depends upon the temperature,
the nature of the solvent, and the structure of the imine.