Syntheses of C20 13α steroidal progestagens

DOI: 10.1248/cpb.22.1140

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 1140 - 1144 (1974)

Update date:2022-08-02

Topics:

Authors:

Goto Goto

Sudo Sudo

Nambara Nambara

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

Article abstract of DOI:10.1248/cpb.22.1140

Full text of DOI:10.1248/cpb.22.1140

NII-Electronic Library Service

Products guided by the article

Product name:19-nor-pregna-1,3,5⁽¹⁰⁾-trien-20-yne-3,17-diol

Cas No:1665-61-8

R&D Labs maybe for 1665-61-8

Acorn PharmaTech Co., Ltd

Contact:86-25-58619180

Address:Nanjing High-Tech Zone 10 Xinghuo Road Pukou District Nanjing, Jiangsu 210061 The People's Republic of China
HEBEI BRANT PHARMACEUTICAL

Contact:+86-0311-84455288-844

Address:Mayu Industrial Park, Jinzhou, Hebei, China.
Suzhou Ryan Pharmachem Technology Co.,Ltd

Contact:+86-0512-68780025

Address:B-301,No.2 Taishan Road,Suzhou New District,Jiangsu,P.R. China
Beijing Top Science biological technology co., LTD

Contact:+86-13439059536

Address:15-1705 jre three mile, Beijing 100000,CHINA
H&Y International Group Ltd

Contact:+86-571-86491666

Address:SHI XIANG ROAD

Relevant to this article

Chemoenzymatic Synthesis of Sertraline

Doi:10.1002/ejoc.201901810
(2020)
Design and synthesis of chromogenic thiopeptolide substrates as MetAPs active site probes

Doi:10.1016/j.bmc.2004.03.044
(2004)
Structure activity relationships of new inhibitors of mammalian 2,3-oxidosqualene cyclase designed from isoquinoline derivatives

Doi:10.1248/cpb.50.316
(2002)
Pd(II)-catalyzed and diethylzinc-mediated asymmetric umpolung allylation of aldehydes in the presence of chiral phosphine-Schiff base type ligands

Doi:10.1016/j.tetasy.2010.06.039
(2010)
Synthesis of the indolizino[7,6- c ]quinoline alkaloid isaindigotidione

Doi:10.1021/ol101890t
(2010)
Rhodium(II)-Catalyzed Annulative Coupling of β-Ketothioamides with α-Diazo Compounds: Access to Highly Functionalized Thiazolidin-4-ones and Thiazolines

Doi:10.1021/acs.joc.0c00378
(2020)

Article Doi