Issue 7, 2012

Gold-catalyzed tandem reaction in water: an efficient and convenient synthesis of fused polycyclic indoles

Abstract

This report describes the gold-catalyzed synthesis of fused polycyclic indoles from substituted 2-(1H-indol-1-yl) alkylamines and alkynoic acids in water under microwave irradiation. This protocol proceeds in high atom economy and leads to the generation of two rings, together with the formation of one new C–C bond and two new C–N bonds in a single operation. The advantages of the method include a short reaction time, excellent yield, easy work-up, and the use of microwave irradiation and an environmentally benign solvent.

Graphical abstract: Gold-catalyzed tandem reaction in water: an efficient and convenient synthesis of fused polycyclic indoles

Supplementary files

Article information

Article type
Paper
Submitted
28 Feb 2012
Accepted
10 Apr 2012
First published
13 Apr 2012

Green Chem., 2012,14, 1888-1895

Gold-catalyzed tandem reaction in water: an efficient and convenient synthesis of fused polycyclic indoles

E. Feng, Y. Zhou, F. Zhao, X. Chen, L. Zhang, H. Jiang and H. Liu, Green Chem., 2012, 14, 1888 DOI: 10.1039/C2GC35293A

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