960化工网
Ugi and Passerini reactions enable the incorporation of ΔAA into N-alkylated peptides and depsipeptides†
Odette Concepción,Francisco J. Peñaloza,Jhon Jairo López,Gustavo Cabrera-Barjas,Claudio A. Jiménez,Márcio W. Paixão,Alexander F. de la Torre
New Journal of Chemistry Pub Date : 05/12/2022 00:00:00 , DOI:10.1039/D2NJ01545E
Abstract

This work renders operational simplicity under mild conditions to synthesize some N-alkylated peptides and depsipeptides containing olefins. A sequential one-pot protocol merging a multicomponent reaction with oxidative elimination of phenylselenoxide allows the formation of α,β and β,γ olefin containing peptides and depsipeptides. Consequently, the regioselective construction of α,β-dehydrobutyrine and α,β-dehydro-homophenylalanine was possible using the Ugi four-component reaction; meanwhile, the Passerini three-component reaction produces the β-enamide preferably.

Graphical abstract: Ugi and Passerini reactions enable the incorporation of ΔAA into N-alkylated peptides and depsipeptides
平台客服
平台客服
平台在线客服