Constituents of Rhizoma nupharis. 23. The absolute configuration of nuphamine.

DOI: 10.1248/cpb.13.1365

Source and publish data:

Chemical and pharmaceutical bulletin p. 1365 - 1368 (1965)

Update date:2022-08-05

Topics:

Authors:

Arata Arata

Ohashi Ohashi

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

Article abstract of DOI:10.1248/cpb.13.1365

Full text of DOI:10.1248/cpb.13.1365

NII-Electronic Library Service

Products guided by the article

Product name:(-)Nuphamin

Cas No:34168-04-2

R&D Labs maybe for 34168-04-2

Shanxi Tongji Pharmaceuticals Co., Ltd.

Contact:+86-359-3024784

Address:Xikuang South Road, Ruicheng County , Shanxi
Xian Lyphar Biotech Co., Ltd.

Contact:0086-29-89196322

Address:North of the Fifth Keji Road, Hi-Tech Industrial Zone, Xi'an City, Shaanxi Province, China
Suzhou Time-chem Technologies Co., Ltd.

Contact:0512-63983931/68086856

Address:No. 1326 of Binhe Road, New District, Suzhou, Jiangsu, P. R. China
SHANXI XINTIANYUAN PHARMACEUTICAL CO., LTD.

website:http://www.tychemical.com

Contact:0086-358-3521713 3521715

Address:No. 1 Yintong Road, Shanxi Jiaocheng Economic Development Zone, Xiajiaying Town, Jiaocheng County, Lvliang City, Shanxi Province, China
Zhejiang Newfine Industry Co.,Ltd.

Contact:+86-573-82262042

Address:No.225,Dongqing Road, garoms@163.com

Relevant to this article

Crystalline films of interdigitated structures formed via amidinium-carboxylate interactions at the air-water interface

Doi:10.1021/ja002597o
(2001)
C₂-symmetric bissulfoximines as ligands in copper-catalyzed enantioselective Diels-Alder reactions

Doi:10.1021/ol027273e
(2003)
Catalytic Assessment of Copper(I) Complexes and a Polymer Analog towards the One-Pot Synthesis of Imines and Quinoxalines

Doi:10.1002/ejic.201900555
(2019)
An efficient method of synthesizing optically pure N-Boc-4-bromo-N-methyl-1-tosyl-D-tryptophan methyl ester, a key intermediate in the synthesis of optically active ergot alkaloids

Doi:10.3987/COM-00-9137
(2001)
Synthesis and in vitro antibacterial activities of novel conformationally restricted hygromycin A analogues

Doi:10.1016/S0960-894X(97)00307-7
(1997)
Improved Nitroaldol Reactions and Reductive Routes to Vicinal Aminoalcohols

Doi:10.1002/hlca.19810640732
(1981)

Article Doi