A new synthesis of 6,7 benzomorphan

DOI: 10.1248/cpb.25.1106

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 1106 - 1108 (1977)

Update date:2022-08-03

Topics:

Authors:

Shiotani

Kometani

Futsukaichi

Mitsuhashi

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

Article abstract of DOI:10.1248/cpb.25.1106

Full text of DOI:10.1248/cpb.25.1106

NII-Electronic Library Service

Products guided by the article

Product name:(+/-)-normetazocine

Cas No:16671-00-4

R&D Labs maybe for 16671-00-4

Shenzhen Sunrising Industry Co., ltd.

Contact:+86 755 86571158 / 86571159 / 86571160

Address:2108 ZHENYE INT. BUSINESS CENTER,NO.3101-90 QIANHAI RD, NANSHAN,SHENZHEN, CHINA
Beijing Zhongshuo Pharmaceutical T & D Co.,Ltd

Contact:0086-10-64430626

Address:ea No 16, HEPINGLI,DONGCHENG DISTRICT,BEIJING,P.R.CHINA.
Shouguang Nuomeng Chemical Co., Ltd.

Contact:+86-536-5119508/18363669993

Address:Hou Zhen Industrial Park, Shouguang, Shandong, China
Shaanxi King Stone Enterprise Company Limited

Contact:86-29-88353805,13609285751

Address:.209 Keji Road Hi-Tech industrial Develpment Zone .Xian China
Puyang Huicheng Electronic Material Co., Ltd

website:http://huichengchem.weba.testwebsite.cn/index_en.html

Contact:+86-393-8910800

Address:West Section Shengli Road, Puyang457000, China

Relevant to this article

A novel NAE/UAE dual inhibitor LP0040 blocks neddylation and ubiquitination leading to growth inhibition and apoptosis of cancer cells

Doi:10.1016/j.ejmech.2018.05.027
(2018)
Facile Synthesis of 3-N-Alkyl Pyrimidin-2,4-diones from N-Sulfonyloxy Maleimides and Amines

Doi:10.1021/acs.orglett.5b02079
(2015)
Large sulfur-nitrogen heterocycles: Preparation of the sulfur imides S(n)NH (n = 8, 9, 11) and structures of S₈NH and S₉NH

Doi:10.1002/anie.199625371
(1996)
Mannich biscyclizations. Total synthesis of (-)-ajmalicine

Doi:10.1021/ja00141a004
(1995)
Synthesis and properties of pyrimido[4,5-a]- and pyrido[4,3-a]carbazole derivatives

Doi:10.1007/s11172-005-0202-y
(2004)
A Stereoselective Route to 1-Chloro-1-halo-Enynes, Versatile Precursors for the Synthesis of Chloroenediynes and Enetriynes

Doi:10.1016/0040-4039(95)00612-G
(1995)

Article Doi