
Journal of Organic Chemistry p. 6098 - 6104 (1990)
Update date:2022-07-29
Topics:
Lee, Chai-Ho
Kohn, Harold
The utility of α-sulfamidoalkylation processes for the generation of sulfamides has been examined.Select aryl-substituted sulfamides were prepared and then treated with acid.Both intra- and intermolecular α-sulfamidoalkylation transformations were observed to proceed in moderate to good yields.The pathways for these reactions are discussed.The generality of these processes has been demonstrated using N,N'-di(aryl-substituted)sulfamides, and the utility of these reactions was examined for the preparation of cyclic sulfamides of novel structure.
View Morewebsite:http://www.guarson.com
Contact:+86-523-88059600,+86-13805268803
Address:Room B1006,Yafang Building,Jiangyan Avenue,Jiangyan District, Taizhou City,Jiangsu,China
Contact:+44 (0)161 367 9441
Address:
Contact:+1 (647) 918 5848
Address:2343 BRIMLEY RD., Suite 250
Hefei TNJ chemical industry co.,ltd
website:https://www.tnjchem.com
Contact:+86-551-65418695
Address:B911 Xincheng Business Center, Qianshan Road, Hefei Anhui China
Nanjing Norris Pharm Technology Co., Ltd.
Contact:+86-13901585132
Address:2 Qiande Road, Jiangning sciencepark Hi-Tech Zone, Nanjing, P.R.China
Doi:10.1021/ol200914j
(2011)Doi:10.1002/cjoc.201190083
(2011)Doi:10.1246/cl.2010.956
(2010)Doi:10.1055/s-0030-1258439
(2011)Doi:10.1007/s10593-011-0693-4
(2011)Doi:10.1016/j.catcom.2019.105784
(2019)