Combinatorial Synthesis of C(2), C(3)-Disubstituted 3-Hydroxypropionamides Utilizing Baylis-Hillman Reactions on Solid Support

Abstract
A four-step reaction protocol for multiple polymer-supported synthesis of structurally diverse α,β-disubstituted 3-hydroxypropionamides 10 has been developed. Variable building blocks were recruited from three monomer pools: primary/secondary amines and aryl aldehydes, the latter of which underwent incorporation into target molecules via Baylis-Hillman reactions. The potential of our approach is demonstrated by machine-assisted assemblage of a small prototype library.

This publication has 0 references indexed in Scilit: