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 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.
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| 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 ÎAA 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 |