Issue 57, 2017

Direct intramolecular amination of tryptophan esters to prepare pyrrolo[2,3-b]indoles

Abstract

A metal-free iodine-catalyzed intramolecular amination has been developed for the practical synthesis of pyrrolo[2,3-b]indoles from readily available tryptophan esters. The transformation has been applied to a wide array of substrates and can be performed on gram scale under very mild conditions.

Graphical abstract: Direct intramolecular amination of tryptophan esters to prepare pyrrolo[2,3-b]indoles

Supplementary files

Article information

Article type
Communication
Submitted
23 May 2017
Accepted
22 Jun 2017
First published
26 Jun 2017

Chem. Commun., 2017,53, 8050-8053

Direct intramolecular amination of tryptophan esters to prepare pyrrolo[2,3-b]indoles

Z. Yang, T. Tian, Y. Du, S. Li, C. Chu, L. Chen, D. Li, J. Liu and B. Wang, Chem. Commun., 2017, 53, 8050 DOI: 10.1039/C7CC03983B

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