Issue 91, 2015

Synthesis of benzofulvenes through chemoselective Sonogashira and Barluenga couplings of ortho ethynyl-N-tosylhydrazones and cycloisomerization

Abstract

Chemoselective synthesis of ortho ethynylhydrazones 7 derived from 2-iodoacetophenone via a Sonogashira coupling is reported for the first time. In this challenging transformation, a site-selective coupling in the presence of a hydrazone function was developed. These compounds represent useful intermediates for the synthesis of benzofulvenes through a sequence of palladium-catalyzed cross-coupling and palladium-catalyzed 5-exo-dig cyclization.

Graphical abstract: Synthesis of benzofulvenes through chemoselective Sonogashira and Barluenga couplings of ortho ethynyl-N-tosylhydrazones and cycloisomerization

Supplementary files

Article information

Article type
Paper
Submitted
21 Jul 2015
Accepted
21 Aug 2015
First published
24 Aug 2015

RSC Adv., 2015,5, 74391-74398

Author version available

Synthesis of benzofulvenes through chemoselective Sonogashira and Barluenga couplings of ortho ethynyl-N-tosylhydrazones and cycloisomerization

J. Aziz, J. Brion, M. Alami and A. Hamze, RSC Adv., 2015, 5, 74391 DOI: 10.1039/C5RA14459K

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