Issue 21, 1978

New synthesis of dienals

Abstract

Addition of sodium derivatives of allyl alcohols (2) to phenylthioacetylene (1) forms adducts (3) which on oxidation and pyrolysis undergo Claisen rearrangement and elimination of benzenesulphenic acid to yield the 2,4-dienals (6).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1978, 924-925

New synthesis of dienals

R. C. Cookson and R. Gopalan, J. Chem. Soc., Chem. Commun., 1978, 924 DOI: 10.1039/C39780000924

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