In:
Angewandte Chemie International Edition, Wiley, Vol. 60, No. 13 ( 2021-03-22), p. 7275-7282
Kurzfassung:
Arylation of carbonyls, one of the most common approaches toward alcohols, has received tremendous attention, as alcohols are important feedstocks and building blocks in organic synthesis. Despite great progress, there is still a great gap to develop an ideal arylation method featuring mild conditions, good functional group tolerance, and readily available starting materials. We now show that electrochemical arylation can fill the gap. By taking advantage of synthetic electrochemistry, commercially available aldehydes (ketones) and benzylic alcohols can be readily arylated to provide a general and scalable access to structurally diverse alcohols (97 examples, 〉 10 gram‐scale). More importantly, convergent paired electrolysis, the ideal but challenging electrochemical technology, was employed to transform low‐value alcohols into more useful alcohols. Detailed mechanism study suggests that two plausible pathways are involved in the redox neutral α‐arylation of benzylic alcohols.
Materialart:
Online-Ressource
ISSN:
1433-7851
,
1521-3773
DOI:
10.1002/anie.202015230
Sprache:
Englisch
Verlag:
Wiley
Publikationsdatum:
2021
ZDB Id:
2011836-3
ZDB Id:
123227-7
