The conversion of berberine into (+/-)-alpha- and (+/-)-beta-hydrastine.

DOI: 10.1021/ja00437a057

Source and publish data:

Journal of the American Chemical Society p. 6714 - 6715 (1976)

Update date:2022-07-31

Topics:

Authors:

Moniot Moniot

Shamma Shamma

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

Article abstract of DOI:10.1021/ja00437a057

Full text of DOI:10.1021/ja00437a057

Products guided by the article

Product name:1,2,3,4-tetrahydro-1-(3,4-dimethoxy-2-methoxycarbonylbenzoyl)-2-methyl-6,7-(methylenedioxy)isoquinoline

Cas No:71734-53-7

R&D Labs maybe for 71734-53-7

Allicon Pharmaceuticals,Inc.

Contact:+86-519-86339586，13584329896

Address:Changzhou Scientific and Education Park
Huaian Double Win Chemicals Co.,Ltd.

Contact:+86-13511538872

Address:Blk 43,Greenland Century Town,Huaian District, Huaian City,Jiangsu Province,China
Xinchang Jiu Xin Pharmaceutical Co., Ltd

website:http://www.jiuxinpharm.com

Contact:86 137 5756 8585

Address:Poyang industry Park
Nantong Kaixin Pharma Chemical Co.,Ltd.

Contact:86-513-85250786

Address:2-1103 Huachen Mansion, 111 Gongnong Road,Nantong, Jiangsu, China
QINGDAO HONG JIN CHEMICAL CO.,LTD.

website:http://www.hongjinchem.com

Contact:+86-532-83657313

Address:2ND Building, 8 Shangqing Road, Qingdao, Shandong Province, China.

Relevant to this article

Simple, Efficient, High Yield Syntheses of Substituted and Unsubstituted 5-Benzoylbarbituric Acids, and Their Corresponding Schiff Base Phenylhydrazones

Doi:10.1002/jhet.5570410214
(2004)
Doi:10.1016/S0008-6215(00)82123-0
(1974)
Doi:10.1007/BF00950986
()
Di- And trifluorobenzenes in reactions with Me₂em (E = P, N; M = SiMe₃, SnMe₃, Li) reagents: Evidence for a concerted mechanism of aromatic nucleophilic substitution

Doi:10.1002/ejoc.200900880
(2010)
Novel lipophilic analogues from 2,4-D and Propanil herbicides: Biological activity and kinetic studies

Doi:10.1016/j.chemphyslip.2020.104947
(2020)
Metabolites of bird's nest fungi. Part II. Diterpenoid metabolites of Cyathus earlei Lloyd

Doi:10.1139/v79-543
(1979)

Article Doi