Issue 52, 2022

Synthesis of allylanilines via scandium-catalysed benzylic C(sp3)–H alkenylation with alkynes

Abstract

The ortho-selective benzylic C(sp3)–H alkenylation of 2-methyl tertiary anilines with internal alkynes has been achieved for the first time by using a half-sandwich scandium catalyst. This protocol provides a straightforward route for the synthesis of a new family of 2-allylaniline derivatives, featuring broad substrate scope, 100% atom-efficiency, high yields, and high chemo-, regio-, and stereoselectivity.

Graphical abstract: Synthesis of allylanilines via scandium-catalysed benzylic C(sp3)–H alkenylation with alkynes

Supplementary files

Article information

Article type
Communication
Submitted
03 May 2022
Accepted
31 May 2022
First published
31 May 2022

Chem. Commun., 2022,58, 7257-7260

Synthesis of allylanilines via scandium-catalysed benzylic C(sp3)–H alkenylation with alkynes

W. Zhou, X. Cong, M. Nishiura and Z. Hou, Chem. Commun., 2022, 58, 7257 DOI: 10.1039/D2CC02489F

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