Issue 29, 2020

Heat- or light-induced acylarylation of unactivated alkenes towards 3-(α-acyl) indolines

Abstract

A heat- or photoredox/iron dual catalysis-enabled dehydrogenative acylarylation of N-allyl anilines leading to 2-substituted 3-(α-acyl) indolines with a quaternary stereogenic center is presented, with unactivated alkenic bonds as radical acceptors and simple aldehydes as radical precursors. This reaction features high yields, a broad substrate scope, and a great exo selectivity, and gram-scale syntheses could be readily carried out.

Graphical abstract: Heat- or light-induced acylarylation of unactivated alkenes towards 3-(α-acyl) indolines

Supplementary files

Article information

Article type
Paper
Submitted
29 May 2020
Accepted
07 Jul 2020
First published
08 Jul 2020

Org. Biomol. Chem., 2020,18, 5660-5665

Heat- or light-induced acylarylation of unactivated alkenes towards 3-(α-acyl) indolines

Y. Li, F. Ying, T. Fu, R. Yang, Y. Dong, L. Lin, Y. Han, D. Liang and X. Long, Org. Biomol. Chem., 2020, 18, 5660 DOI: 10.1039/D0OB01105C

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements