Tetrahedron Letters p. 3261 - 3264 (1992)
Update date:2022-07-30
Topics: Synthesis alkenes Aziridines N-H
Vedejs, Edwin
Sano, Hiroshi
Electron-rich alkenes are converted into N-methoxyaziridines by treatment with HN(OCH3)2 and trimethylsilyl triflate.Reduction with Li/ammonia affords the N-H aziridines. Key words: Aziridine; N-methoxyaziridine; N-methoxycaprolactam; dimethoxyamine; nitrenium ion
View Morewebsite:http://www.josunpharma.com
Contact:+86-311-80715268 80766839
Address:No.39, Zhaiying Street, Shijaizhuang,Hebei,China
Ceresking Ecology & Technology co.,ltd
Contact:86 22 66218397
Address:Room 1613, Zheshang Mansion, No. 1988, Yingbin Avenue, Binhai New District, Tianjin,China.
Contact:+86-512-56795332
Address:No227 Shuanglong Rd, Fenghuang, Zhangjiagang
Shanghai Sungo Technology Chemical Co., Ltd
Contact:0086-21-51385579
Address:Room2010, F/20, Tonghua Plaza, NO 345 Jinxiang Road, Jinqiao Export Processing Zone, Shanghai, 201206 P.R.CHINA
Contact:86-310-8067016
Address:East Fuhua Road,Tiexi Chemical Industrial Estate,Hebei,China
Doi:10.1016/j.bmc.2013.01.069
(2013)Doi:10.1021/ic400240b
(2013)Doi:10.1002/ejoc.202001233
(2021)Doi:10.1007/s10593-013-1218-0
(2013)Doi:10.1002/zaac.201200357
(2012)Doi:10.1016/S0040-4039(00)96852-7
(1987)
