Syntheses of catechol estrogen 16,17 ketols, new and potential metabolites

DOI: 10.1248/cpb.21.2725

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 2725 - 2732 (1973)

Update date:2022-08-03

Topics:

Authors:

Nambara Nambara

Kawarada

Asama Asama

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.21.2725

Full text of DOI:10.1248/cpb.21.2725

NII-Electronic Library Service

Products guided by the article

Product name:Acetic acid (13S,16R,17R)-2,3-bis-benzyloxy-13-methyl-6,7,8,9,11,12,13,14,15,16-decahydro-20-oxa-cyclopropa[16,17]cyclopenta[a]phenanthren-17-yl ester

Cas No:51478-06-9

R&D Labs maybe for 51478-06-9

Hangzhou Pharma & Chem Co.,Ltd.

Contact:+86-571-87040515

Address:No,139Qingchun Rd
Nanjing Qirui Material Co., Ltd.

Contact:+86-25-52320053

Address:F4-5, #17 Building, Chuang Yi Yuan, No.6 Guanghua East Street, Nanjing, 210007 P.R.China
Xiamen Hisunny Chemical Co.,Ltd

website:http://www.hisunnychem.com

Contact:+86-592-3327115

Address:Unit 603,No.879,Xiahe Road,Meixin Building,Xiamen,China
HangZhou HuaYe Chemical Technology Co.,Ltd

Contact:+86-13505815007

Address:hangzhou
shijiazhuang baisheng chem co.; ltd

Contact:86-0311-80790826

Address:shijiazhuang hebei

Relevant to this article

Reactions of odd-electron cobaltacycles: Characterization of a persistent 17-electron anionic intermediate in electron-transfer-catalyzed (ETC) substitution reactions

Doi:10.1021/om990246g
(1999)
Doi:10.1002/hlca.19430260528
(1943)
Syntheses and mesomorphic and luminescent properties of disubstituted polyacetylenes bearing biphenyl pendants

Doi:10.1021/ma049094d
(2004)
Enantioselective Nickel-Catalyzed Hydrocyanation using Chiral Phosphine-Phosphite Ligands: Recent Improvements and Insights

Doi:10.1002/adsc.201500644
(2015)
Synthesis of 1,8-naphthyridines from 2-aminonicotinaldehydes and terminal alkynes

Doi:10.1016/j.tetlet.2016.03.070
(2016)
A Photochemical Organocatalytic Strategy for the α-Alkylation of Ketones by using Radicals

Doi:10.1002/anie.201915814
(2020)

Article Doi