Issue 26, 2017

Tertiary amine self-catalyzed intramolecular Csp3–H functionalization with in situ generated allenes for the formation of 3-alkenyl indolines

Abstract

A novel methodology for the synthesis of 3-alkenyl indolines through the reaction of in situ generated allenes with N-benzylic Csp3–H has been developed. The reaction was realized by Pd(0) catalyzed allenylation of propargyl carbonate with organoboron and subsequent tertiary amine self-catalyzed Csp3–H functionalization in a one-pot process. Control reactions suggested that the substrate itself might also serve as a Lewis base for the N-benzylic Csp3–H functionalization.

Graphical abstract: Tertiary amine self-catalyzed intramolecular Csp3–H functionalization with in situ generated allenes for the formation of 3-alkenyl indolines

Supplementary files

Article information

Article type
Communication
Submitted
01 Jan 2017
Accepted
09 Mar 2017
First published
09 Mar 2017

Chem. Commun., 2017,53, 3721-3724

Tertiary amine self-catalyzed intramolecular Csp3–H functionalization with in situ generated allenes for the formation of 3-alkenyl indolines

Y. Zhao, M. Xu, Z. Zheng, Y. Yuan and Y. Li, Chem. Commun., 2017, 53, 3721 DOI: 10.1039/C7CC00005G

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