Issue 0, 1966

The acid-catalysed rearrangement of diterpene hydrocarbons. Part I. Kaurene, isoatisirene, stachene, and trachylobane

Abstract

Stachene, trachylobane, and kaurene have been converted into mixtures of atisirene, isoatisirene, kaurene, and isokaurene. Isoatisirene furnishes an equilibrium mixture of starting material and atisirene.

The conversion of stachene into isoatisirene involves a novel 1,3-hydride shift in a bicyclo[3,2,1]octane system.

Article information

Article type
Paper

J. Chem. Soc. C, 1966, 2319-2322

The acid-catalysed rearrangement of diterpene hydrocarbons. Part I. Kaurene, isoatisirene, stachene, and trachylobane

R. A. Appleton, A. J. McAlees, A. McCormick, R. McCrindle and R. D. H. Murray, J. Chem. Soc. C, 1966, 2319 DOI: 10.1039/J39660002319

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