Issue 73, 2013
From the journal:

Chemical Communications

FeCl3 mediated intramolecular olefin-cationcyclization of cinnamates for the synthesis of highly substituted indenes†‡

Dattatraya H. Dethe*a  and  Ganesh M. Murhadea  

* Corresponding authors

a Department of Chemistry, Indian Institute of Technology Kanpur, Kanpur 208016, India
E-mail: ddethe@iitk.ac.in
Fax: +91-512-2597436
Tel: +91-512-2596537

Abstract

Highly substituted indene derivatives were readily prepared in excellent yields with high regioselectivity under very mild reaction conditions by the FeCl3 mediated intramolecular olefin-cationic cyclization of cinnamates.

Graphical abstract: FeCl3 mediated intramolecular olefin-cation cyclization of cinnamates for the synthesis of highly substituted indenes

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Article information

DOI
https://doi.org/10.1039/C3CC43159B
Article type
Communication
Submitted
29 Apr 2013
Accepted
05 Jul 2013
First published
09 Jul 2013

Chem. Commun., 2013,49, 8051-8053

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FeCl3 mediated intramolecular olefin-cation cyclization of cinnamates for the synthesis of highly substituted indenes

D. H. Dethe and G. M. Murhade, Chem. Commun., 2013, 49, 8051 DOI: 10.1039/C3CC43159B

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