Unknown

Dataset Information

0

Photocatalyst-free hydroacylations of electron-poor alkenes and enones under visible-light irradiation.


ABSTRACT: 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 para-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.

SUBMITTER: Palvolgyi AM 

PROVIDER: S-EPMC9491158 | biostudies-literature | 2022 Sep

REPOSITORIES: biostudies-literature

altmetric image

Publications

Photocatalyst-free hydroacylations of electron-poor alkenes and enones under visible-light irradiation.

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]

Similar Datasets

| S-EPMC11905314 | biostudies-literature
| S-EPMC6036985 | biostudies-literature
| S-EPMC7384135 | biostudies-literature
| S-EPMC5238574 | biostudies-literature
| S-EPMC7137949 | biostudies-literature
| S-EPMC7934782 | biostudies-literature
| S-EPMC5550426 | biostudies-other
| S-EPMC9027963 | biostudies-literature
| S-EPMC9084558 | biostudies-literature
| S-EPMC5399282 | biostudies-literature