Issue 24, 2005

A diversity oriented four-component approach to tetrahydro-β-carbolines initiated by Sonogashira coupling

Abstract

A consecutive four-component synthesis of highly-substituted tetrahydro-β-carbolines 6 can be achieved by a coupling-aminatio-aza-annulation-Pictet–Spengler (CAAPS) sequence creating five new σ-bonds and four new stereocenters in a one-pot fashion. The structures were unambiguously supported by X-ray structure analyses.

Graphical abstract: A diversity oriented four-component approach to tetrahydro-β-carbolines initiated by Sonogashira coupling

Supplementary files

Article information

Article type
Paper
Submitted
23 Aug 2005
Accepted
06 Oct 2005
First published
14 Nov 2005

Org. Biomol. Chem., 2005,3, 4382-4391

A diversity oriented four-component approach to tetrahydro-β-carbolines initiated by Sonogashira coupling

A. S. Karpov, F. Rominger and T. J. J. Müller, Org. Biomol. Chem., 2005, 3, 4382 DOI: 10.1039/B511861A

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