Synthesis of 14α-methylcholesterol

DOI: 10.1248/cpb.35.3467

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 3467 - 3469 (1987)

Update date:2022-08-05

Topics:

Authors:

Takahashi

Usami Usami

Takahashi

Okada Okada

Morisaki

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

Article abstract of DOI:10.1248/cpb.35.3467

Full text of DOI:10.1248/cpb.35.3467

Products guided by the article

Product name:14α-methylcholest-5-en-3α-ol

Cas No:115058-86-1

R&D Labs maybe for 115058-86-1

Alway Chem, China

website:http://www.alwaychem.com

Contact:+86-532-8586-4000, 8586-5000

Address:NO.51, TAIPING ROAD, QINGDAO, CHINA. 266001
Arromax Pharmatech Co.,Ltd

website:http://www.arromax.com

Contact:+86-0512-62959601 skype:aimmezhang

Address:Suite 401, Bldg A3, 218 Xinghu St.Suzhou Industrial Park 215123, P.R. China
SuZhou Bichal Biological Technology CO.,LTD

Contact:+86-512-68051130

Address:NO.32 huoju road HI-TECH Industrial development zone SuZhou China
Sino-Japan Chemical Co., Ltd.

website:http://www.sjc.com.tw

Contact:(886) 2-2396-6223

Address:14Fl., No. 99. Sec. 2, Jen Ai Road
SHANGHAI ARCADIA BIOTECHNOLOGY LTD.

Contact:+86-21-61353236

Address:SUITE 901, BUILDING WENSLI, 1378 LU JIA BANG RD, SHANGAHI 200011, P.R.CHINA

Relevant to this article

Morpholine containing CB2 selective agonists

Doi:10.1016/j.bmcl.2009.02.033
(2009)
Siliciumverbindungen mit starken intermolekularen sterischen Wechselwirkungen XXVIII. Neue Cyclotrisilane und Cyclotetrasilane

Doi:10.1016/S0022-328X(00)99789-4
(1987)
Tunable differentiation of tertiary C-H bonds in intramolecular transition metal-catalyzed nitrene transfer reactions

Doi:10.1039/c7cc01235g
(2017)
Doi:10.1039/jr9590000788
(1959)
A new approach to pseudo-sugars from (-)-quinic acid: Facile syntheses of pseudo-β-D-mannopyranose and pseudo-β-D-fructopyranose

Doi:10.1039/c39900000748
(1990)
Design and synthesis of glucose-templated proline-lysine chimera: polyfunctional amino acid chimera with high prolyl cis amide rotamer population

Doi:10.1016/j.carres.2008.12.024
(2009)

Article Doi