A NOVEL SYNTHESIS OF HALOKETENIMINE

DOI: 10.1246/cl.1981.1197

Source and publish data:

Chemistry Letters p. 1197 - 1198 (1981)

Update date:2022-08-02

Topics:

Authors:

Hirao, Toshikazu

Hayashi, Ken-ichiro

Motoyoshiya, Jiro

Ohshiro, Yoshiki

Agawa, Toshio

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

Haloketenimines are prepared by treatment of 2,2-dihaloaziridines with triethylamine in acetonitrile.

Chengdu Chengnuo New-Tech Co., Ltd

Contact:0086-028-85749078

Address:4 Jiuyang road,Jiulong industrial port,Chengdu, China
Shanghai Surseechem Co.,Ltd.

Contact:+86-21-61318535

Address:Building 29,No.2139 Xizha Road, Fengxian District, Shanghai
Dongying J&M Chemical Co., Ltd,

Contact:546-8551108

Address:Room 1219, Zisheng Mansion, Zibo Road, Dongying, Shandong, China
CHINA MEHECO CORPORATION

Contact:+86-10-67147360/67107388

Address:No.18 Guangming Zhongjie, Chongwen District, Beijing, 100061, China
Xian Changyue Biological Technology Co., Ltd.

website:https://www.xachangyue.com/

Contact:+86-029-88211911

Address:Keji Road NO.70

Doi:10.1039/c39740000948
(1974)
Doi:10.1016/S0040-4039(00)71892-2
(1975)
Doi:10.1021/jo00864a016
(1976)
Design and development of pyrrole carbaldehyde: An effective pharmacophore for enoyl-ACP reductase

Doi:10.1007/s00044-016-1517-y
(2016)
Doi:10.1246/cl.1975.319
(1975)
Asymmetric Cyclization of N-Sulfonyl Alkenyl Amides Catalyzed by Iridium/Chiral Diene Complexes

Doi:10.1021/acs.orglett.6b01954
(2016)