Jump to main content
Jump to site search

Issue 13, 2014
Previous Article Next Article

Applications of Bartoli indole synthesis

Author affiliations

Abstract

In 1989, the reaction of vinyl magnesium halides with ortho-substituted nitroarenes leading to indoles was discovered. This reaction is now frequently reported as the “Bartoli reaction” or the “Bartoli indole synthesis” (BIS). It has rapidly become the shortest and most flexible route to 7-substituted indoles, because the classical indole syntheses generally fail in their preparation. The flexibility of the Bartoli reaction is great as it can be extended to heteroaromatic nitro derivatives and can be run on solid support. This review will focus on the use of the Bartoli indole synthesis as the key step in preparations of complex indoles, which appeared in the literature in the last few years.

Graphical abstract: Applications of Bartoli indole synthesis

Back to tab navigation

Article information


Submitted
24 Jan 2014
First published
10 Apr 2014

Chem. Soc. Rev., 2014,43, 4728-4750
Article type
Review Article
Author version available

Applications of Bartoli indole synthesis

G. Bartoli, R. Dalpozzo and M. Nardi, Chem. Soc. Rev., 2014, 43, 4728
DOI: 10.1039/C4CS00045E

Social activity

Search articles by author

Spotlight

Advertisements