Issue 5, 2015

Efficient synthesis of α- and δ-carbolines by sequential Pd-catalyzed site-selective C–C and twofold C–N coupling reactions

Abstract

Two concise and efficient approaches were developed for the synthesis of α- and δ-carboline derivatives. The success of the synthesis relies on site-selective Suzuki–Miyaura reactions of 1-chloro-2-bromopyridine or 2,3-dibromopyridine with 2-bromophenylboronic acid and subsequent cyclization with amines which proceeds by twofold Pd-catalyzed C–N coupling reactions.

Graphical abstract: Efficient synthesis of α- and δ-carbolines by sequential Pd-catalyzed site-selective C–C and twofold C–N coupling reactions

Supplementary files

Article information

Article type
Paper
Submitted
20 Oct 2014
Accepted
13 Nov 2014
First published
13 Nov 2014

Org. Biomol. Chem., 2015,13, 1375-1386

Author version available

Efficient synthesis of α- and δ-carbolines by sequential Pd-catalyzed site-selective C–C and twofold C–N coupling reactions

T. Q. Hung, T. T. Dang, J. Janke, A. Villinger and P. Langer, Org. Biomol. Chem., 2015, 13, 1375 DOI: 10.1039/C4OB02226B

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