137958-85-1Relevant articles and documents
Palladium-Catalyzed Hydroaminocarbonylation of Alkynes with Tertiary Amines via C-N Bond Cleavage
Gao, Bao,Huang, Hanmin
supporting information, p. 6260 - 6263 (2017/11/24)
An efficient strategy for the cleavage of the C-N bond of tertiary amines was developed with DTBP as an oxidant, in which the cleaved H atom and amine moiety were successfully transferred to the desired products. This strategy has enabled an efficient palladium-catalyzed hydroaminocarbonylation of alkynes with tertiary amines. Notably, the catalyst loading could be lowered from 5 to 0.1 mol %, which represents the lowest catalyst loading among the reported work on carbonylation via C-N bond activation.
Organic Iodide Aided Carbonylation of Terminal Acetylenes with Palladium Catalyst
Torii, Sigeru,Okumoto, Hiroshi,Sadakane, Masahiro,He Xu, Long
, p. 1673 - 1676 (2007/10/02)
Carbonylation of various terminal acetylenes in the presence of a catalytic amount of organic iodides or amine * HI salt and palladium complexes was found to produce 2-substituted acrylamides in good yields under mild conditions (5 atm, 120 deg C, 6h).