Abstract
H-Phosphonate diesters undergo transesterification with amino alcohols to afford as primary products the mixed and the symmetrical H-phosphonate esters. Alcohols react similarly but only in the presence of an external base or in a basic solvent. The rate and the course of transesterification strongly depend on the reaction conditions, the reactivity of the H-phosphonate diester used, and the nature of the amino alcohol.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have