Issue 42, 2018

Photocatalytic acylarylation of unactivated alkenes with diaryliodonium salts toward indanones and related compounds

Abstract

A novel photocatalytic acylarylation of unactivated alkenes using diaryliodonium salts as the arylation reagent is described. The reaction produces a variety of 2-benzyl indanones, 3,4-dihydronaphthalen-1(2H)-ones, and 2,3-dihydroquinolin-4(1H)-ones in promising yields with excellent diastereoselectivity under very mild conditions, which may be appealing for the synthesis of biologically active molecules.

Graphical abstract: Photocatalytic acylarylation of unactivated alkenes with diaryliodonium salts toward indanones and related compounds

Supplementary files

Article information

Article type
Communication
Submitted
02 Apr 2018
Accepted
03 May 2018
First published
03 May 2018

Chem. Commun., 2018,54, 5373-5376

Photocatalytic acylarylation of unactivated alkenes with diaryliodonium salts toward indanones and related compounds

Y. Chen, C. Shu, F. Luo, X. Xiao and G. Zhu, Chem. Commun., 2018, 54, 5373 DOI: 10.1039/C8CC02636J

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