Issue 0, 1967

Dienone–phenol type rearrangements. Part II. Synthesis of a bicyclic phenol

Abstract

1,2,3,4-Tetrahydro-1,1,5-trimethylnaphthalene-2,6-diol, obtained from acid-catalysed rearrangement of a di-hydroxy-octalone and also from photochemical rearrangement of a bicyclic dienone, has been synthesised as its mono-O-methyl ether by an independent route.

Article information

Article type
Paper

J. Chem. Soc. C, 1967, 2677-2678

Dienone–phenol type rearrangements. Part II. Synthesis of a bicyclic phenol

B. R. Davis and L. J. Forrest, J. Chem. Soc. C, 1967, 2677 DOI: 10.1039/J39670002677

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