Issue 12, 1988

Studies of [3,3]sigmatropic rearrangements: rearrangement of 3-(4-p-tolyloxybut-2-ynyloxy)[1]benzopyran-2-one

Abstract

3-(4-p-Tolyloxybut-2-ynyloxy)[1]benzopyran-2-one (1), when refluxed in chlorobenzene, ethyl benzene, or xylene, gave exclusively 1-(p-tolyloxymethyl)pyrano[2,3-c][1]benzopyran-5(3H)-one (2), whereas through an ionic or radical pathway 2-methyl-1-(p-tolyloxymethyl)furo[2,3-c][1]benzopyran-4-one (3) was the exclusive product.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1988, 777-779

Studies of [3,3]sigmatropic rearrangements: rearrangement of 3-(4-p-tolyloxybut-2-ynyloxy)[1]benzopyran-2-one

K. C. Majumdar, R. N. De, A. T. Khan, S. K. Chattopadhyay, K. Dey and A. Patra, J. Chem. Soc., Chem. Commun., 1988, 777 DOI: 10.1039/C39880000777

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