Issue 14, 2005
From the journal:

Chemical Communications

Directed palladation: fine tuning permits the catalytic 2-alkenylation of indoles

Elena Capito,ab   John M. Browna  and  Alfredo Riccib  

a Chemical Research Laboratory, Mansfield Road, Oxford, UK
E-mail: bjm@herald.ox.ac.uk
Fax: +44 1865 280002

b Dipartimento di Chimica Organica “A. Mangini”, Universitá di Bologna, Viale Risorgimento 4, Bologna, Italy
E-mail: ricci@ms.fci.unibo.it

Abstract

A C–H activating Pd-catalysed alkenylation of indole is regiospecific for 2-substitution when the nitrogen carries a 2-pyridylmethyl substituent.

Graphical abstract: Directed palladation: fine tuning permits the catalytic 2-alkenylation of indoles

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Article information

DOI
https://doi.org/10.1039/B417035K
Article type
Communication
Submitted
09 Nov 2004
Accepted
17 Dec 2004
First published
17 Feb 2005

Chem. Commun., 2005, 1854-1856

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Directed palladation: fine tuning permits the catalytic 2-alkenylation of indoles

E. Capito, J. M. Brown and A. Ricci, Chem. Commun., 2005, 1854 DOI: 10.1039/B417035K

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