
Journal of Organic Chemistry p. 4897 - 4901 (1988)
Update date:2022-09-26
Topics: Catalyst Reduction NITROSATION High-yield Regiospecific Synthesis
Okamoto, Tadashi
Kobayashi, Kenji
Oka, Shinzaburo
Tanimoto, Shigeo
The title reaction of substituted styrenes, 1-phenyl-1,3-butadiene, and some cyclic aryl-conjugated ethylenes proceeds smoothly at room temperature, affording the corresponding oximes in moderate to nearly quantitative yields.The reaction mechanism is discussed on the basis of the formation of an alkylcobalt intermediate and its subsequent reaction with ethyl nitrite.
View MoreSuzhou Jingye Medicine & Chemical Co., Ltd
Contact:+86-512-66658588
Address:No. 88, Sanlian Street, Jinfeng Road, Suzhou New District, Jiangsu Province, P. R. China
Contact:+86-717-6370352
Address:168 Chengdong Avenue, Yichang, Hubei 443003, P. R.China
Contact:+86-13914766747
Address:Floors 21&22, Jin Cheng Tower, No. 216 Middle Longpan Road, Nanjing
Hangzhou Haiqiang Chemical Co.,Ltd.
Contact:+86-571-86960370
Address:Add: 5/F, Around Town North Road,No. 10, Hangzhou, Zhejiang,China
Zhengzhou Xinlian Chemical Tech Co. ,Ltd
Contact:0371-65771781 021-52042910
Address:H Part, Building I, No. 700 Gonglu Road, Pudong New Area, Shanghai
Doi:10.1021/ja01531a032
(1959)Doi:10.1021/ja00255a077
(1987)Doi:10.1021/jo000214z
(2000)Doi:10.1021/ja00257a046
(1987)Doi:10.1021/jo00233a016
(1987)Doi:10.1021/ol102504b
(2010)