Versatile intramolecular reactions starting from a conformationally restricted epoxyalcohol

DOI: 10.1016/S0040-4039(00)79585-2

Source and publish data:

Tetrahedron Letters p. 3009 - 3012 (1992)

Update date:2022-08-05

Topics:

Authors:

Hart Hart

Vacher Vacher

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Article abstract of DOI:10.1016/S0040-4039(00)79585-2

The novel epoxyalcohol, 3, has been converted, using a variety of stereoselective intramolecular cyclisation reactions, to several highly substituted cyclohexane derivatives. In addition carbon disulphide has been shown to be a powerful intramolecular sul

Full text of DOI:10.1016/S0040-4039(00)79585-2

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