20120-26-7Relevant articles and documents
Bromodimethylsulfonium bromide mediated Michael addition of amines to electron deficient alkenes
Khan, Abu T.,Parvin, Tasneem,Gazi, Sarifuddin,Choudhury, Lokman H.
, p. 3805 - 3808 (2007)
Bromodimethylsulfonium bromide has been found to be an efficient catalyst for the Michael addition of a wide variety of amines to electron deficient alkenes at room temperature. The protocol is very simple and chemoselective. Aliphatic and benzylic amines undergo conjugate addition within a very short period under solvent-free conditions and provide excellent yields of products.
SEGREGATED FLUORINATED ESTERS
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Page/Page column 29, (2016/05/24)
Segregated fluorinated esters are described that are useful as dielectric fluids in electrical devices and as heat transfer agents.
Guanidine-based task-specific ionic liquids as catalysts for aza-Michael addition under solvent-free conditions
Ying, Anguo,Zheng, Ming,Xu, Haidan,Qiu, Fangli,Ge, Changhua
experimental part, p. 883 - 890 (2012/04/17)
An efficient and facile protocol for aza-Michael addition of aliphatic and aromatic amines to electron-deficit alkenes using [TMG][Lac] as catalyst under solvent-free conditions was established.