Issue 17, 1969

Preparation and solvolysis of dispirotetraenediones

Abstract

Dispiro[5,0,5,4]hexadeca-1,4,8,11-tetraene-3,10-dione and a lower homologue, prepared by oxidation of the appropriate diphenols, decompose in neutral alcoholic solutions to give benzylic ethers arising, apparently, from quinone methide intermediates.

Article information

Article type
Paper

J. Chem. Soc. D, 1969, 996-996

Preparation and solvolysis of dispirotetraenediones

M. N. Afzal, A. D. Allbutt, A. Jordaan and G. W. Kirby, J. Chem. Soc. D, 1969, 996 DOI: 10.1039/C29690000996

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