Issue 71, 2018

A copper(ii)-catalyzed annulative formylation of o-alkynylanilines with DMF: a single-step strategy for 3-formyl indoles

Abstract

In this paper, a copper(II)-catalyzed reaction of o-alkynylanilines with dimethylformamide (DMF) in the presence of oxygen has been developed for synthesizing multisubstituted 3-formyl indole scaffolds. This one-pot reaction proceeds through a cascade 5-endo-dig cyclization followed by formylation to construct 1,2-disubstituted 3-formyl indoles. The key aspects of this synthesis method are the broad substrate scope (with 38 examples), and well tolerating various functional groups. In addition, a detailed mechanism has been proposed, where DMF may serve as a carbon source for the in situ C3 formylation of the obtained indole derivatives.

Graphical abstract: A copper(ii)-catalyzed annulative formylation of o-alkynylanilines with DMF: a single-step strategy for 3-formyl indoles

Supplementary files

Article information

Article type
Paper
Submitted
07 Nov 2018
Accepted
30 Nov 2018
First published
07 Dec 2018
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2018,8, 40968-40973

A copper(II)-catalyzed annulative formylation of o-alkynylanilines with DMF: a single-step strategy for 3-formyl indoles

B. Ganesan, G. C. Senadi, B. Guo, M. Hung and W. Lin, RSC Adv., 2018, 8, 40968 DOI: 10.1039/C8RA09214A

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