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Issue 9, 1978
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Formation of ketones from steroidal thioacetals: some sulphur containing steroids

Abstract

A selection of steroidal thioacetals has been oxidised to the disulphinyl derivatives which are readily decomposed by alkali with the regeneration of the parent ketones.

The condensation of propane-1,3-dithiol with 2α-bromo-3-oxosteroids furnishes the corresponding 2,3-dihydrodithiins.

Structures have been assigned to the condensation products of ethane-1,2-dithiol and a steroidal 4,6-diene-3-one and 1,4,6-trien-3-one.

An improved synthesis of SS-trimethylene 1,3-bis(toluene-p-thiosulphonate) is reported.

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Article type: Paper
DOI: 10.1039/P19780001011
Citation: J. Chem. Soc., Perkin Trans. 1, 1978,0, 1011-1014
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    Formation of ketones from steroidal thioacetals: some sulphur containing steroids

    P. R. Heaton, J. M. Midgley and W. B. Whalley, J. Chem. Soc., Perkin Trans. 1, 1978, 0, 1011
    DOI: 10.1039/P19780001011

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