ARGÜELLO JUAN ELIAS
Artículos
Título:
Multi-step Synthesis of Organic Selenides under Visible-light Irradiation: A Continuous Flow Approach
Autor/es:
HEREDIA, ADRIÁN; SORIA-CASTRO, SILVIA M.; CASTRO-GODOY, WILLBER D.; LEMIR, IGNACIO DANIEL; LÓPEZ-VIDAL, MARTÍN; BISOGNO, FABRICIO R.; ARGÜELLO, JUAN E.; OKSDATH-MANSILLA, GABRIELA
Revista:
ORGANIC PROCESS RESEARCH & DEVELOPMENT
Editorial:
AMER CHEMICAL SOC
Referencias:
Año: 2020
ISSN:
1083-6160
Resumen:
he potential application of multi-step continuous-flow systems has had a great impact on the syntheses of active pharmaceutical ingredients (APIs), natural products and commodity chemicals. In this report, the highly efficient combination of a chemical reduction and photochemical Csp2-H activation reaction for selenylation of biologically relevant electron-rich arenes was achieved by means of continuous-flow process. Firstly, the reduction of alkyl and aryl selenocyanates by Rongalite® was achieved giving the corresponding diselenides; secondly, photo-activation of the Se-Se bond resulted in the selenylation of electron-rich arenes, both steps from good to excellent yield. In all cases, the reaction time was shortened, and isolated yields were improved when compared to batch reaction conditions. Furthermore, connecting both reactions in a multi-step continuous flow sequence was possible even when reductive and photo-oxidative transformations were coupled.