Synthesis of (17R)- and (17S)- 17-hydroxy- 14, 15-secoandrost-4-en-15-yn- 3-one and the X-ray crystal structure of the (17S)-diastereomer

DOI: 10.1016/0039-128X(95)00062-U

Source and publish data:

Steroids p. 491 - 496 (1995)

Update date:2022-08-05

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Authors:

Sherwin Sherwin

Covey Covey

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Article abstract of DOI:10.1016/0039-128X(95)00062-U

(17R,S)-17-Hydroxy-14,15-secoandrost-4-en-15-yn-3-one has been shown previously to be a mechanism-based inactivator of rat liver 3α- hydroxysteroid dehydrogenase. This manuscript describes the synthesis of this diastereomeric 14,15-secosteroid from [2S-(2

Full text of DOI:10.1016/0039-128X(95)00062-U

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Product name:1-<(4-methylphenyl)sulfonyl>-L-proline (17S)-3-oxo-14,15-secoandrost-4-en-15-yn-17-yl ester

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