Journal of Organic Chemistry p. 3673 - 3676 (1980)
Update date:2022-08-11
Topics:
Nakajima, Masayuki
Anselme, Jean-Pierre
The reaction of N-nitrosamides with lithium aluminium hydride results mainly in attack of hydride at the carbonyl group to give the aldehyde and the diazotate ion (syn ?) as the primary products.Products resulting from N-nitrene fragmentation (by reduction of the nitroso group) and from hydride-induced denitrosation were also characterized.
View MoreChengdu CSH Pharmaceutical Co.,ltd
Contact:+86-(28)-85321971
Address:Block B,New Hope Int. Tian Fu New District, Chengdu, Sichuan, China
Chengda Pharmaceuticals Co., Ltd.
Contact:+86-573-84601188
Address:hengshan Road 5# in Jiashan, zhejiang
Hangzhou Yanshan Chemical Co.,Ltd.
Contact:86-571- 87698076
Address:Room 1001, #1 Building, Zhongtian MCC, No.2 Youzhinong, Wenyi West Road, Xihu District, Hangzhou, China
Guangzhou Swan Chemical Co., Ltd.
Contact:+86-20-31075659
Address:NO.301, Hong ba fang investment BLDG 1,Guan chong village,Shiqi town,Panyu district,Guangzhou
Jiangsu Taihu New Materials Holding Co., Ltd
Contact:+86-519-86160108
Address:Xueyan Town, Changzhou City, Jiangsu Province, 213169, China
Doi:10.1016/S0040-4039(01)85244-8
(1972)Doi:10.1016/j.ejmech.2020.113067
(2021)Doi:10.1055/s-1986-31491
(1986)Doi:10.1002/anie.201902418
(2019)Doi:10.24820/ark.5550190.p010.488
(2018)Doi:10.1002/ardp.19743071119
(1974)