Issue 1, 1991

Rhodium carbenoid mediated cyclisations. Part 7. Synthesis and coupling reactions of 2-substituted 3-oxooxepanes

Abstract

A range of 2-substituted oxepanes 3 has been prepared from δ-lactones via rhodium(II) acetate catalysed cyclisation of the intermediate diazo alcohols 2. The phenylsulphonyloxepane 3e and the oxepane phosphonate 3f are versatile substrates for further elaboration, and are readily converted into substituted oxepanes 1214.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1991, 1-7

Rhodium carbenoid mediated cyclisations. Part 7. Synthesis and coupling reactions of 2-substituted 3-oxooxepanes

M. J. Davies, C. J. Moody and R. J. Taylor, J. Chem. Soc., Perkin Trans. 1, 1991, 1 DOI: 10.1039/P19910000001

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