Issue 19, 2018

Rh(iii)-Catalyzed regioselective C–H [4 + 2] C-annulation of vinyl enaminones with alkynes to form polysubstituted salicylaldehydes

Abstract

A Rh(III)-catalyzed regioselective C–H [4 + 2] C-annulation reaction of vinyl enaminones with alkynes is developed to provide sterically congested polysubstituted salicylaldehydes. This reaction shows relatively broad substrate scope with good functional group tolerance. The applications of this method to prepare useful synthetic precursors and bioactive skeletons are also exemplified.

Graphical abstract: Rh(iii)-Catalyzed regioselective C–H [4 + 2] C-annulation of vinyl enaminones with alkynes to form polysubstituted salicylaldehydes

Supplementary files

Article information

Article type
Research Article
Submitted
24 Jul 2018
Accepted
02 Sep 2018
First published
03 Sep 2018

Org. Chem. Front., 2018,5, 2875-2879

Rh(III)-Catalyzed regioselective C–H [4 + 2] C-annulation of vinyl enaminones with alkynes to form polysubstituted salicylaldehydes

Y. Zhao, Q. Zheng, C. Yu, Z. Liu, D. Wang, J. You and G. Gao, Org. Chem. Front., 2018, 5, 2875 DOI: 10.1039/C8QO00759D

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