A practical synthesis of 3-substituted Δ(3,6(6))-steroids as new potential 5α-reductase inhibitor

DOI: 10.1016/S0960-894X(98)00339-4

Source and publish data:

Bioorganic and Medicinal Chemistry Letters p. 1949 - 1952 (1998)

Update date:2022-08-11

Topics:

Authors:

Tian, Weisheng

Zhu, Zheng

Liao, Qingjiang

Wu, Yikang

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1016/S0960-894X(98)00339-4

A new and practical synthetic approach to 3-substituted Δ(3,5(6))- Steroids, as potential 5α-reductase inhibitor, is described. The key step involves Pd-catalyzed coupling reaction of steroid 3-enol 5H-3-oxo- octafluoropentanosulfonates. 3-Phenylacetyleny

Full text of DOI:10.1016/S0960-894X(98)00339-4

Products guided by the article

Product name:Epristeride

Cas No:119169-78-7

R&D Labs maybe for 119169-78-7

shanghai payne pharm co.,ltd.

Contact:+86-021-58123769

Address:No.780 of Cailun Road,Zhangjiang Hi-tech Park,Pudong,Shanghai
Zhejiang Allied Chemical Co.,Ltd

Contact:18967038207

Address:Area A-30, High-tech Industrial Park, Quzhou, Zhejiang, China.
Hangzhou GreenCo Science & Technology Co., Ltd.

Contact:86-571-88257303

Address:1713 Room,Jingui Building,Gudun Road,Xihu District,Hangzhou,China
Jining kaikesi Industry and trade Co.Ltd【Cancel license】

Contact:86--13287237433

Address:Jining City Yanzhou District Daan Town AnQiuFu Village
ZHUHAI HAIRUIDE BIOSCIENCE AND TECHNOLOGY CO.,LTD

website:http://www.zhhairuide.com

Contact:+8613326687259/+86-756-7789199

Address:No.10 Yonghui Road

Relevant to this article

Doi:10.1021/jo01184a006
(1944)
Aquachlororuthenium(III) catalysis in the oxidation of substituted 4-oxo-4-arylbutanoic acids by bromate in acid medium: A kinetic and mechanistic study and validity of linear free-energy relationships

Doi:10.1007/s11243-011-9523-x
(2011)
Synthesis of SiC nanorods using floating catalyst

Doi:10.1016/S0038-1098(01)00181-8
(2001)
Doi:10.1007/BF00473107
()
Porous Carbon-Hosted Atomically Dispersed Iron–Nitrogen Moiety as Enhanced Electrocatalysts for Oxygen Reduction Reaction in a Wide Range of pH

Doi:10.1002/smll.201703118
(2018)
Syntheses of (R)- and (S)-enantiomeric 1,1,1-trifluoromethyl-2-alkanols with high enantiomeric purity controlled through derivatization with l-menthyl phthalate

Doi:10.1016/j.tetlet.2015.09.073
(2015)

Article Doi