Scholarly article on 16β-Brom-androst-5-en-3β,17β-diol 5986-84-5 from Journal of the Chemical Society C: Organic p. 484 - 488

DOI: 10.1039/j39660000484

Source and publish data:

Journal of the Chemical Society C: Organic p. 484 - 488 (1966)

Update date:2022-08-03

Topics:

Authors:

Hewett,C.L.

Savage,D.S.

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

Article abstract of DOI:10.1039/j39660000484

Full text of DOI:10.1039/j39660000484

View Article Online / Journal Homepage / Table of Contents for this issue

View Article Online

Products guided by the article

Product name:16β-Brom-androst-5-en-3β,17β-diol

Cas No:5986-84-5

R&D Labs maybe for 5986-84-5

Nanyang Tianhua pharmaceutical Co.,Ltd.

Contact:+8618639816203

Address:Longsheng Industrial Park
HangZhou HuaYe Chemical Technology Co.,Ltd

Contact:+86-13505815007

Address:hangzhou
Liaoyang hengye Chemical Co., Ltd.

Contact:86-419-5850866

Address:North Old Xiaoxiao Road,Yantai District, Dengta, Liaoyang, Liaoning, China
Liaoyang Xinyou Chemical Products Co.,Ltd.

Contact:+86-419-5165433 13604191870

Address:Huishang Road6-1, Hongwei District, Liaoyang, Liaoning, China
Shandong Topscience Biotech Co., Ltd.

Contact:0633-2619278

Address:No. 98 Lanshan West Road, Lanshan District, Rizhao, Shandong Province, P.R. of China

Relevant to this article

A stereoselective route to trisubstituted olefines from β - lactones

Doi:10.1016/S0040-4039(01)99187-7
(1968)
Highly regioselective ring opening of epoxides and aziridines using cerium(III) chloride

Doi:10.1016/S0040-4039(01)00622-0
(2001)
The Synthesis and Single-crystal X-Ray Structure of the First Example of a Tridentate, Di-orthometallated Triphenyl Phosphite Complex

Doi:10.1039/c39950002049
(1995)
Doi:10.1007/BF00757985
()
Asymmetric Cross [10+2] Cycloadditions of 2-Alkylidene-1-indanones and Activated Alkenes under Phase-Transfer Catalysis

Doi:10.1002/chem.201904930
(2020)
Design, synthesis and antimycobacterial activity evaluation of natural oridonin derivatives

Doi:10.1016/j.bmcl.2014.04.119
(2014)

Article Doi

DOI: 10.1039/j39660000484