Issue 12, 2003
From the journal:

Chemical Communications

A convenient two step protocol for the synthesis of cyclopentenones and indanones, including an asymmetric variant†

Daniel J. Kerr,a   Christiane Metjea  and  Bernard L. Flynn‡*a  

* Corresponding authors

a Department of Chemistry, The Faculties, Australian National University, Canberra ACT, 0200, Australia

Abstract

A one-pot palladium mediated hydrostannylation/cross-coupling protocol is used to give direct access to cross-conjugated dienones that can be utilized in Nazarov cyclizations to afford highly substituted cyclopentenones and indanones, including an asymmetric variant.

Graphical abstract: A convenient two step protocol for the synthesis of cyclopentenones and indanones, including an asymmetric variant

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Article information

DOI
https://doi.org/10.1039/B211845A
Article type
Communication
Submitted
28 Nov 2002
Accepted
07 Mar 2003
First published
12 May 2003

Chem. Commun., 2003, 1380-1381

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A convenient two step protocol for the synthesis of cyclopentenones and indanones, including an asymmetric variant

D. J. Kerr, C. Metje and B. L. Flynn, Chem. Commun., 2003, 1380 DOI: 10.1039/B211845A

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