Ugi and Passerini reactions enable the incorporation of Delta AA into N-alkylated peptides and depsipeptides
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 SOC CHEMISTRY |
| Fecha de publicación: | 2022 |
| Página de inicio: | 11502 |
| Página final: | 11509 |
| DOI: |
10.1039/d2nj01545e |
| Notas: | ISI |