Issue 23, 2008

Tandem addition-cyclization reactions of 2-alkynylbenzenamines with isocyanates catalyzed by PdCl2

Abstract

Tandem addition-cyclization reactions of 2-alkynylbenzenamines with isocyanates catalyzed by palladium chloride are described. This reaction is performed in the presence of 10 mol% of palladium chloride in THF at 80 °C, which provides an efficient and practical route for the synthesis of 1,2-disubstituted indoles.

Graphical abstract: Tandem addition-cyclization reactions of 2-alkynylbenzenamines with isocyanates catalyzed by PdCl2

Supplementary files

Article information

Article type
Paper
Submitted
14 Jul 2008
Accepted
01 Sep 2008
First published
15 Oct 2008

Org. Biomol. Chem., 2008,6, 4406-4412

Tandem addition-cyclization reactions of 2-alkynylbenzenamines with isocyanates catalyzed by PdCl2

S. Ye, Q. Ding, Z. Wang, H. Zhou and J. Wu, Org. Biomol. Chem., 2008, 6, 4406 DOI: 10.1039/B812015C

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