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

Penaloza, Francisco J.

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.

Más información

Título según WOS: Ugi and Passerini reactions enable the incorporation of Delta AA into N-alkylated peptides and depsipeptides
Título según SCOPUS: Ugi and Passerini reactions enable the incorporation of ΔAA 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 final: 11509
Idioma: English
DOI:

10.1039/d2nj01545e

Notas: ISI, SCOPUS