Issue 13, 2015

DMSO/Tf2O-mediated cross-coupling of tryptamine with substituted aniline to access C3a–N1′-linked pyrroloindoline alkaloids

Abstract

The cross-coupling of tryptamine with substituted aniline to access C3a–nitrogen-linked pyrroloindolines has been developed via the consecutive cyclization of tryptamine with DMSO/Tf2O and the substitution of 3a-pyrroloindolylthionium intermediate with aniline. The use of 2,3-dihydrotryptamine instead of aniline enabled easy access to 3a-(1-indolyl)pyrroloindoline and the concise synthesis of C3a–N1′-linked pyrroloindoline alkaloid (±)-psychotriasine was accomplished.

Graphical abstract: DMSO/Tf2O-mediated cross-coupling of tryptamine with substituted aniline to access C3a–N1′-linked pyrroloindoline alkaloids

Supplementary files

Article information

Article type
Communication
Submitted
30 Jan 2015
Accepted
18 Feb 2015
First published
18 Feb 2015

Org. Biomol. Chem., 2015,13, 3863-3865

Author version available

DMSO/Tf2O-mediated cross-coupling of tryptamine with substituted aniline to access C3a–N1′-linked pyrroloindoline alkaloids

M. Tayu, T. Ishizaki, K. Higuchi and T. Kawasaki, Org. Biomol. Chem., 2015, 13, 3863 DOI: 10.1039/C5OB00190K

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