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

Xinchang Jiu Xin Pharmaceutical Co., Ltd

website:http://www.jiuxinpharm.com

Contact:86 137 5756 8585

Address:Poyang industry Park
Zhejiang Chemicals Import & Export Corporation (ZHECHEM)

Contact:+86-571-87046953

Address:No. 37, Qingchun Road
Pale Palm Imex

Contact:+36(21)2523420

Address:Head office: 1102 Budapest, SZENT LASZLO TER 24/B. 1/1., HUNGARY / CHINA
Kaiping Genuine Biochemical Pharmaceutical Co.,Ltd.

Contact:+86-750-2881198

Address:No.1, Xinke Road, Shatang Town, Kaiping, Guangdong Province, P.R.China
Shanghai Topchem Co., LTD

website:http://www.shtopchem.com/

Contact:0086-0576-87776998

Address:room no 1608,xuhui business building yude road,xujiahui street, xuhui district

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