Studies on the alkaloids of the papaveraceae. XVII. The alkaloids of Corydalis incisa. X. The structure of (+) 14 epicorynolin

DOI: 10.1248/cpb.21.1096

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 1096 - 1102 (1973)

Update date:2022-07-29

Topics:

Authors:

Takao Takao

Bersch Bersch

Takao Takao

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

Article abstract of DOI:10.1248/cpb.21.1096

Full text of DOI:10.1248/cpb.21.1096

NII-Electronic Library Service

Products guided by the article

Product name:11-Epicorynolin-O-acetat

Cas No:42881-67-4

R&D Labs maybe for 42881-67-4

Jiangxi Global Natural Spice Co., Ltd.

website:https://www.jxhqxl.com/

Contact:+86-796-8106598

Address:No.89, Wenshan Road,South Industrial Park, Jishui County,Jiangxi Province
Hefei Lifeon Pharmaceutical Co., Ltd.

Contact:+86-551-65328450

Address:No522 Wangjiang West Road
Alway Chem, China

website:http://www.alwaychem.com

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

Address:NO.51, TAIPING ROAD, QINGDAO, CHINA. 266001
Wuhan Pengo Technology.,Ltd.

Contact:+86-27-67841589

Address:Add: 999 Gaoxin Road, Donghu New Technology Development Zone, Wuhan City, Hubei, China
Changzhou Ruiping Chemical Co., Ltd

website:http://www.wishchem.com

Contact:+86-519-82324280

Address:No.288-1 Huacheng Road, Jintan

Relevant to this article

Efficient synthesis of 2-deoxy-L-erythro-pentose (2-deoxy-L-ribose) from L-arabinose

Doi:10.1016/S0008-6215(01)00329-9
(2002)
Thiophenol-Catalyzed Visible-Light Photoredox Decarboxylative Couplings of N-(Acetoxy)phthalimides

Doi:10.1021/acs.orglett.6b03300
(2016)
Substrate-dependent nonlinear effects in proline-thiourea-catalyzed aldol reactions: Unraveling the role of the thiourea co-catalyst

Doi:10.1002/chem.200902678
(2010)
Adenine nucleotide analogues locked in a Northern methanocarba conformation: Enhanced stability and potency as P2Y₁ receptor agonists

Doi:10.1021/jm010538v
(2002)
Doi:10.1007/BF02988250
(1954)
Stereochemical Differences in Fluorocyclopropyl Amides Enable Tuning of Btk Inhibition and Off-Target Activity

Doi:10.1021/acsmedchemlett.0c00249
(2020)

Article Doi