Analogues of androgen hormones with inverted configuration at carbons 5, 9, and 10.

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F02%3A57020084" target="_blank" >RIV/61388963:_____/02:57020084 - isvavai.cz</a>

Result on the web

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DOI - Digital Object Identifier

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Result language

angličtina

Original language name

Analogues of androgen hormones with inverted configuration at carbons 5, 9, and 10.

Original language description

On catalytic hydrogenation of Westphalen-type steroids, four isomers were formed.The product distribution was affected by the nature of the C-3 substituent. A chair conformation of A, B, and C rings was found in all of the products with the exception ofthe 9.alfa.,10.alfa.-adduct whose B ring adopts a twist boat conformation. The products were utilized for the synthesis of dihydrotestosterone.

Czech name

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Czech description

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Type

J_x - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

CEP classification

CC - Organic chemistry

OECD FORD branch

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Project

<a href="/en/project/GA505%2F94%2F0009" target="_blank" >GA505/94/0009: Biological Effects of Antiandrogens in the Mammary Gland: Structure - Activity Relationship</a><br>

Continuities

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>Z - Vyzkumny zamer (s odkazem do CEZ)

Publication year

2002

Confidentiality

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Name of the periodical

Steroids

ISSN

0039-128X

e-ISSN

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Volume of the periodical

67

Issue of the periodical within the volume

N/A

Country of publishing house

US - UNITED STATES

Number of pages

14

Pages from-to

57-70

UT code for WoS article

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EID of the result in the Scopus database

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