Issue 15, 1998

A novel reductive cyclization of arylmethylidenemalononitrile promoted by samarium diiodide

Abstract

The intermolecular and intramolecular reductive coupling reactions of arylmethylidenemalononitriles induced by SmI2 have been studied. The configuration of the cyclodimerization products, 4,5-trans-isomers of 2-amino-1,3,3-tricyano-4,5-diarylcyclopentenes, has been confirmed by X-ray analysis and a possible reaction mechanism is proposed.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1998, 2399-2402

A novel reductive cyclization of arylmethylidenemalononitrile promoted by samarium diiodide

L. Zhou and Y. Zhang, J. Chem. Soc., Perkin Trans. 1, 1998, 2399 DOI: 10.1039/A802510J

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