Ontology highlight
ABSTRACT:
SUBMITTER: Palvolgyi AM
PROVIDER: S-EPMC9491158 | biostudies-literature | 2022 Sep
REPOSITORIES: biostudies-literature
Pálvölgyi Ádám Márk ÁM Ehrschwendtner Florian F Schnürch Michael M Bica-Schröder Katharina K
Organic & biomolecular chemistry 20220921 36
Herein we present a photocatalyst- and additive-free radical hydroacylation of electron-poor double bonds under mild reaction conditions. Using 4-acyl-Hantzsch ester radical reservoirs, various Michael acceptors, enones and <i>para</i>-quinone methide substrates could be used. The protocol enabled further derivatizations and it could also be extended to a few unactivated alkenes. Moreover, the nature of the radical process was also investigated. ...[more]