Some reactions of 16α,17α-oxido-5α-cholestane derivatives, synthesis of 17α-hydroxycholest-4-en-3-one

DOI: 10.1016/0039-128X(94)90123-6

Source and publish data:

Steroids p. 335 - 340 (1994)

Update date:2022-07-31

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Authors:

Velgova, Helena

Kasal, Alexander

Budinsky, Milo

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Article abstract of DOI:10.1016/0039-128X(94)90123-6

Careful epoxidation of the Δ¹⁶-olefins 3 and 4 yielded 16α,17α- epoxides 5 and 6 which were reduced by lithium aluminium hydride, oxidized, and dehydrated to 17α-hydroxycholest-4-en-3-one 20, i.e., an epitestosterone homolog containing a well t

Full text of DOI:10.1016/0039-128X(94)90123-6

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