Alkylated steroids. Part 3. The 21-alkylation of 20-oxopregnanes and synthesis of a novel anti-inflammatory 16α,17α,21-trimethyl steroid (Org 6216)
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1981/P1/P19810002306
Cited by 10 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Optimization of the synthesis of 21-benzylidene-substituted steroids and pitfalls of the Claisen-Schmidt condensation;Russian Chemical Bulletin;2023-12
2. Key structures in the synthesis of steroid antitumor agents. Methods for upbuilding the 17β-pregnane side chain of 3-methoxy-19-norpregna-1,3,5(10)-trien-20-ones with and without an additional 16α,17α-carbocycle;Russian Chemical Bulletin;2022-08
3. Hormone Therapeutics - Systemic Hormonal Preparations, Excluding Reproductive Hormones and Insulins (H);Ullmann's Encyclopedia of Industrial Chemistry;2017-11-30
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5. Microbial hydroxylation of 16α,17α-dimethyl-17β-(l-oxopropyl)androsta-l,4-dien-3-one to rimexolone by Curvularia lunata AS 3.4381;Journal of Molecular Catalysis B: Enzymatic;2007-07
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