Scholarly article on 5α-Androstan-6-one 3676-06-0 from Journal of the Chemical Society C: Organic p. 2421 - 2426

DOI: 10.1039/j39700002421

Source and publish data:

Journal of the Chemical Society C: Organic p. 2421 - 2426 (1970)

Update date:2022-08-03

Topics:

Authors:

Jones,D.N.

Grayshan,R.

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

Article abstract of DOI:10.1039/j39700002421

Full text of DOI:10.1039/j39700002421

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

View Article Online

Products guided by the article

Product name:5α-Androstan-6-one

Cas No:3676-06-0

R&D Labs maybe for 3676-06-0

Chengdu D-Innovation Pharmaceutical Co., Ltd

Contact:86-28-85105536

Address:1001, B6, No.88 Keyuan South Road, Chengdu Hi-Tech Zone
Hubei Sibo Technology Co.,Ltd.

Contact:0715-6597222

Address:Pan Jia Wan fan Lake Chemical Industrial Park ,Xianning City, Hubei, China
Tianjin Crest Pharmaceutical R&D Co., Ltd. （Tianjin Yao Technology Development Co., Ltd.）(expird)

Contact:+86-22-66211386

Address:Building B5-405, No, 80 4th Avenue, TEDA, Tianjin, China P.R. 300457
Shenyang Mole pharmaceutical Technology Development Co.,Ltd

Contact:+86-24-31204918/13889278616

Address:No.44, wanliutang road, shenhe District of Shenyang
Jiangsu Chiatai Qingjiang Pharmaceutical Co.,Ltd

Contact:+86-517-86283327

Address:9 North Hantai Road, Huaian, China

Relevant to this article

Rh(III)-Catalyzed Oxidative Annulation Leading to Substituted Indolizines by Cleavage of C(sp²)-H/C(sp³)-H Bonds

Doi:10.1021/acs.orglett.6b01181
(2016)
Coordinatively unsaturated W(IV)-bis(pyridine) complexes, a reactive source of W(IV)

Doi:10.1021/ic010195r
(2001)
Doi:10.1016/S0040-4020(01)93205-3
(1964)
Catalytic asymmetric cyclopropanation of heteroaryldiazoacetates

Doi:10.1021/jo015617t
(2001)
Metal free Lewis acid promoted one-pot synthesis of 14-aryl-14H dibenzo [a,j] xanthenes and their simple biological evolution

Doi:10.1016/j.tetlet.2017.07.037
(2017)
Doi:10.1021/ja00763a037
(1972)

Article Doi

DOI: 10.1039/j39700002421