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 MoreContact:+86-532-80762375
Address:No. 6, Hongkong Middle Road, Qingdao, China
Huangshan Honghui Pharm Technology Co., Ltd.(expird)
website:http://www.honghuichem.com
Contact:18855958372
Address:Qingshan Wan No.1,Nanyuan Kou,SheXian Huangshan City,Anhui Province
Shanghai Zhihua ChemTech Co., Ltd.
Contact:+86-13774313779
Address:Room 817 Suite B 3333 Shenjiang Road
Contact:86-21-57725962
Address:shanghai
Shandong Xiangde Biotechnology Co., Ltd
Contact:+86 -15066639877
Address:Sanba street
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)
