Catalytic activation of C-H and C-C bonds of allylamines via olefin isomerization by transition metal complexes
(matrix presented) The metal-catalyzed reaction of olefins with allylamines bearing coordination sites (2-pyridyl groups) was studied. With Ru3(CO)12 as catalyst, activation of C-H bonds led to the formation of ketimines that were hydrolyzed to give asymmetric ketones. With [(C8H14)2RhCl]2, both C-H and C-C bonds were activated and symmetric ketones were formed on hydrolysis. The reaction involves double bond migration of the allylamine to form an aldimine.
Jun, Chul-Ho,Lee, Hyuk,Park, Jae-Bum,Lee, Dae-Yon
p. 2161 - 2164
(2008/02/11)
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