Issue 14, 2007

A strategy for the synthesis of 2,3-disubstituted indoles starting from N-(o-halophenyl)allenamides

Abstract

A strategy for the synthesis of 2,3-disubstituted indole derivatives based on an intramolecular carbopalladation–anion capture cascade has been developed, wherein construction of the pyrrole ring and functionalisation of the indole C2 and C3 positions were achieved by extensive use of palladium(0)-catalysed coupling reactions.

Graphical abstract: A strategy for the synthesis of 2,3-disubstituted indoles starting from N-(o-halophenyl)allenamides

Supplementary files

Additions and corrections

Article information

Article type
Communication
Submitted
15 May 2007
Accepted
30 May 2007
First published
19 Jun 2007

Org. Biomol. Chem., 2007,5, 2214-2218

A strategy for the synthesis of 2,3-disubstituted indoles starting from N-(o-halophenyl)allenamides

H. Fuwa and M. Sasaki, Org. Biomol. Chem., 2007, 5, 2214 DOI: 10.1039/B707338K

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