1036572-20-9Relevant articles and documents
Expanding the forefront of strong organic br?nsted acids: Proton-catalyzed hydroamination of unactivated alkenes and activation of au(i) for alkyne hydroamination
Mirabdolbaghi, Roya,Dudding, Travis
, p. 1930 - 1933 (2015)
The synthesis of a solid, bench-stable, strong organic Br?nsted acid with a computed pKa of 0.9 is reported. An X-ray crystal structure and DFT calculations are provided which offer insight into the bonding of this acid. The application of this
Gallium trichloride catalyzed hydroamination of alkynes: Scope, limitation, and mechanistic studies by dft
Li, Lei,Huang, Genping,Chen, Zhou,Liu, Wei,Wang, Xiufang,Chen, Yanmei,Yang, Lijuan,Li, Wu,Li, Yahong
supporting information, p. 5564 - 5572 (2012/11/07)
The successful application of gallium trichloride as a catalyst for the intermolecular hydroamination of alkynes with aromatic amines is reported. The reaction is effective with many aniline derivatives and shows exclusive selectivity for the Markovnikov