Issue 9, 1970

Rotenoid synthesis, by one-carbon insertion, from 2′-hydroxyisoflavones using dimethylsulphoxonium methylide

Abstract

The vinylcoumaranone (V) formed when isoderritol isoflavone (I) reacts with dimethylsulphoxonium methylide (1 mol) is isomerised by pyridine to isorotenone (X): the new rotenoid synthesis has similarities to the biosynthetic route.

Article information

Article type
Paper

J. Chem. Soc. D, 1970, 563a-563a

Rotenoid synthesis, by one-carbon insertion, from 2′-hydroxyisoflavones using dimethylsulphoxonium methylide

L. Crombie, P. W. Freeman and D. A. Whiting, J. Chem. Soc. D, 1970, 563a DOI: 10.1039/C2970000563A

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