Issue 14, 2010

New xanthate-based radical cyclization onto alkynes

Abstract

To bypass the failure of radical cyclization involving a xanthate transfer on alkynes, a new reductive cyclization strategy has been completed with the use of a stoichiometric amount of dilauroyl peroxide in isopropanol. When the starting xanthates are prepared via a Ugi 4-component reaction with propargylamine, exomethylene lactams are formed in good yields.

Graphical abstract: New xanthate-based radical cyclization onto alkynes

Supplementary files

Article information

Article type
Communication
Submitted
18 Nov 2009
Accepted
08 Jan 2010
First published
27 Jan 2010

Chem. Commun., 2010,46, 2489-2491

New xanthate-based radical cyclization onto alkynes

L. El Kaïm, L. Grimaud, L. D. Miranda, E. Vieu, M.-Angeles Cano-Herrera and K. Perez-Labrada, Chem. Commun., 2010, 46, 2489 DOI: 10.1039/B924207D

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