Journal of the Chemical Society. Chemical communications p. 149 - 150 (1983)
Update date:2022-08-17
Topics:
Niel, Johannes C. G. van
Pandit, Upendra K.
Reduction of N-cyclopropylmethylenephenylamine by 3,5-diethoxycarbonyl-2,6-dimethyl-1,4-dihydropyridine (Hantzsch ester) results in the exclusive formation of N-cyclopropylmethylaniline, whereas reduction with triphenyltin hydride gives both N-cyclopropylmethylaniline and n-butylaniline, a product of cyclopropane ring cleavage.
View MoreLinHai Cina Chemical Co., LTD.
Contact:0576-85580989
Address:Pharma-chem zone,Duqiao,Linhai,Zhejiang,China
Shuanghe Bio-Technology Limited(expird)
Contact:+86-571-61710758,18968016640
Address:Jinqiao north road 916# Fuyang
website:http://www.angchenchem.com
Contact:+86-510-88302099 82327577
Address:Rm. 404/405, Floor 4th, No. 983 FengXiang Road, Wuxi, China
website:https://www.sinoshiny.com/products
Contact:+86-20-62802632;62802633
Address:Room 330 GIGCAS Building,No.511 Kehua Street,Tianhe District
Changzhou BaoKang Pharmaceutical & Chemical Co., Ltd
Contact:(86) 519-88782201 88784080 88785278
Address:Henglin town, changzhou,Jiangsu
Doi:10.1016/S0022-328X(00)81950-6
(1982)Doi:10.1039/c9ra05576b
(2019)Doi:10.1021/jo00253a039
(1988)Doi:10.1021/ja00543a027
(1980)Doi:10.1021/jo00268a010
(1989)Doi:10.1021/ja00480a070
(1978)
