Visible Light-Promoted Friedel-Crafts-Type Chloroacylation of Alkenes to β-Chloroketones

Citations

WEB OF SCIENCE

35
Citations

SCOPUS

36

초록

The photoredox chloroacylation of alkenes has been developed as a substitute for the Friedel-Crafts acylation of alkenes to β-chloroketones. The direct generation of acyl radical species from acid chlorides under the photoredox conditions allows the formation of β-chloroketones without dehydrochlorination with the help of KHCO3. The synthetic utility of the current method is demonstrated in the one-pot synthesis of dihydroisoxazole, dihydropyrazole, and dihydropyrimidine-2-thione in 1 mmol scale.

키워드

CHLOROVINYL KETONES; ACYLATION; CHLORIDES; CHEMISTRY
제목
Visible Light-Promoted Friedel-Crafts-Type Chloroacylation of Alkenes to β-Chloroketones
저자
Patil D.V.; Kim H.Y.; Oh K.
DOI
10.1021/acs.orglett.0c00788
발행일
2020-04
유형
Article
저널명
Organic Letters
권
22
호
8
페이지
3018 ~ 3022