108223-53-6Relevant articles and documents
Bismuth-catalyzed intermolecular hydroamination of 1,3-dienes with carbamates, sulfonamides, and carboxamides
Qin, Hongbo,Yamagiwa, Noriyuki,Matsunaga, Shigeki,Shibasaki, Masakatsu
, p. 1611 - 1614 (2006)
A Bi(OTf)3/Cu(CH3CN)4PF6 system efficiently promoted intermolecular 1:1 hydroamination of 1,3-dienes with various carbamates, sulfonamides, and carboxamides to afford allylic amines in good yield (up to 96%). Re
Heteropoly acids: a green and efficient heterogeneous Br?nsted acidic catalyst for the intermolecular hydroamination of olefins
Yang, Lei,Xu, Li-Wen,Xia, Chun-Gu
, p. 2882 - 2885 (2008/09/21)
Intermolecular hydroamination of non-activated olefins with amides and benzyl carbamate proceeds efficiently in the presence of environmentally benign silicotungstic acid (HSiW) catalyst under mild conditions in air to afford addition products in good to excellent yields.
DERIVATIVES OF SELENIUM DIIMIDE
Barashenkov, G. G.,Derkach, N. Ya.
, p. 1069 - 1074 (2007/10/02)
The reaction of selenium with N-sodio-N-chlorobenzenesulfonamide and N-sodio-N-chloro-p-toluenesulfonamide leads to the formation of derivatives of orthoselenious acid, i.e., bis(N-sodioarylsulfonylamino)selenium dichlorides.