Issue 27, 2012

Synthesis of tetrahydro-β-carbolines via isomerization of N-allyltryptamines: a metal-catalyzed variation on the Pictet–Spengler theme

Abstract

An efficient and broadly applicable alternative to the classical Pictet–Spengler synthesis of tetrahydro-β-carbolines is presented. The method relies on metal-catalyzed isomerization of allylic amines to form reactive iminium intermediates which can be trapped by a tethered indole nucleophile.

Graphical abstract: Synthesis of tetrahydro-β-carbolines via isomerization of N-allyltryptamines: a metal-catalyzed variation on the Pictet–Spengler theme

Supplementary files

Article information

Article type
Communication
Submitted
08 Dec 2011
Accepted
07 Feb 2012
First published
10 Feb 2012

Chem. Commun., 2012,48, 3345-3347

Synthesis of tetrahydro-β-carbolines via isomerization of N-allyltryptamines: a metal-catalyzed variation on the Pictet–Spengler theme

E. Ascic, C. L. Hansen, S. T. Le Quement and T. E. Nielsen, Chem. Commun., 2012, 48, 3345 DOI: 10.1039/C2CC17704H

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