Issue 120, 2015

Facile catalyst-free synthesis of 2-vinylquinolines via a direct deamination reaction occurring during Mannich synthesis

Abstract

A facile catalyst-free method for the synthesis of 2-vinylquinolines via a direct deamination reaction during Mannich synthesis has been developed. Instantaneous hydrogen transfer via a six-membered ring intermediate is proposed as a key step for the direct deamination reaction. This reaction strategy tolerates a broad substrate scope and provides a highly efficient way to synthesize 2-vinylquinolines with adequate yields.

Graphical abstract: Facile catalyst-free synthesis of 2-vinylquinolines via a direct deamination reaction occurring during Mannich synthesis

Supplementary files

Article information

Article type
Communication
Submitted
14 Oct 2015
Accepted
10 Nov 2015
First published
13 Nov 2015

RSC Adv., 2015,5, 99095-99098

Author version available

Facile catalyst-free synthesis of 2-vinylquinolines via a direct deamination reaction occurring during Mannich synthesis

J. Xiao, Y. Huang, Z. Song and W. Feng, RSC Adv., 2015, 5, 99095 DOI: 10.1039/C5RA21304E

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