Ugi and Passerini reactions enable the incorporation of Delta AA into N-alkylated peptides and depsipeptides

Concepcion, Odette; Penaloza, Francisco J.; Lopez, Jhon Jairo; Cabrera-Barjas, Gustavo; Jimenez, Claudio A.; Paixao, Marcio W.; de la Torre, Alexander F.

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 alpha,beta and beta,gamma olefin containing peptides and depsipeptides. Consequently, the regioselective construction of alpha,beta-dehydrobutyrine and alpha,beta-dehydro-homophenylalanine was possible using the Ugi four-component reaction; meanwhile, the Passerini three-component reaction produces the beta-enamide preferably.

Más información

Título según WOS: Ugi and Passerini reactions enable the incorporation of Delta AA into N-alkylated peptides and depsipeptides
Título de la Revista: NEW JOURNAL OF CHEMISTRY
Volumen: 46
Número: 24
Editorial: Royal Society of Chemistry
Fecha de publicación: 2022
Página de inicio: 11502
Página final: 11509
DOI:

10.1039/d2nj01545e

Notas: ISI