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Catalysed sodium borohydride reductions of ortho-nitrocinnamates
Journal of the Chemical Society C: Organic Pub Date : , DOI:10.1039/J39690000713
Abstract

The products obtained when o-nitrocinnamates are reduced by means of sodium borohydride and palladium–charcoal depend on the nature of the solvent used. When ethyl trans-α-cyano-o-nitrocinnamate was reduced by this method, one of the products isolated was 3-cyano-1-hydroxyquinol-2(1H)-one, the formation of which involved a smooth transcis isomerisation.

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