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Issue 62, 2012
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Thermally induced [3+2] cyclization of aniline-tethered alkylidenecyclopropanes: a facile synthetic protocol of pyrrolo[1,2-a]indoles

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Abstract

A facile synthetic method of functionalized pyrrolo[1,2-a]indoles has been developed via a thermally-induced ring-opening and cyclization reaction from aniline-tethered alkylidenecyclopropanes with aldehydes.

Graphical abstract: Thermally induced [3+2] cyclization of aniline-tethered alkylidenecyclopropanes: a facile synthetic protocol of pyrrolo[1,2-a]indoles

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Publication details

The article was received on 07 May 2012, accepted on 11 Jun 2012 and first published on 13 Jun 2012


Article type: Communication
DOI: 10.1039/C2CC33269H
Citation: Chem. Commun., 2012,48, 7696-7698

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    Thermally induced [3+2] cyclization of aniline-tethered alkylidenecyclopropanes: a facile synthetic protocol of pyrrolo[1,2-a]indoles

    K. Chen, Z. Zhang, Y. Wei and M. Shi, Chem. Commun., 2012, 48, 7696
    DOI: 10.1039/C2CC33269H

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