Chemical conversion of corticosteroids to 3α,5α-tetrahydro derivatives. Synthesis of allotetrahydro-11-deoxycortisol glucuronides

DOI: 10.1248/cpb.33.4281

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 4281 - 4287 (1985)

Update date:2022-08-04

Topics:

Authors:

Hosoda Hosoda

Takasaki

Miura Miura

et al. et al.

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

Article abstract of DOI:10.1248/cpb.33.4281

Full text of DOI:10.1248/cpb.33.4281

NII-Electronic Library Service

Products guided by the article

Product name:THS 21-glucuronide

Cas No:103293-13-6

R&D Labs maybe for 103293-13-6

Wuxi Olite Chemical Co., Ltd.

Contact:86-510-82853889

Address:Rm.3732, No.18-2,Yonghe Rd.,Wuxi,Jiangsu,214023,China
Exploiter Molybdenum Co.,Ltd

Contact:86-379-63338609

Address:Jiudian Village,Deting Town,Song County,Luoyang
Zhejiang Kaili Industrial Co., Ltd

Contact:+86-571-85241926

Address:lantian business center,No.18 Moganshan Road
Daqing E-shine Chemical Co.,LTD

Contact:0086-024-31285112

Address:Hongweiyuan area, Ranghulu district
SJZ Chenghui Chemical Co., Ltd.

Contact:86-311-87713916

Address:no.368 youyi north avenue

Relevant to this article

Sulfoxide-directed stereocontrolled access to 2H-chromans: Total synthesis of the (S,R,R,R)-enantiomer of the antihypertensive drug nebivolol

Doi:10.1002/ejoc.200800201
(2008)
Synthesis of pyrrolo[2,1-c][1,4]benzoxazepines. 1. A novel heterocyclic ring system

Doi:10.1002/jhet.5570220429
(1985)
Bioisosteric Replacement of Arylamide-Linked Spine Residues with N-Acylhydrazones and Selenophenes as a Design Strategy to Novel Dibenzosuberone Derivatives as Type i 1/2 p38α MAP Kinase Inhibitors

Doi:10.1021/acs.jmedchem.0c00508
(2020)
CYCLOPENTADIENYLEISEN-KOMPLEXE MIT P(OR3)-LIGANDEN; SYNTHESE UND SPEKTROSKOPISCHE CHARAKTERISIERUNG

Doi:10.1016/0022-328X(85)80248-5
(1985)
Doi:10.1021/ja00752a024
(1971)
An efficient separation method for enol phosphate and corresponding β-ketophosphonate from their mixtures under aqueous conditions

Doi:10.1081/SCC-120021033
(2003)

Article Doi