THE UNPRECEDENTED TRANSFORMATION OF A STERICALLY CROWDED CYCLOPALLADATED SECONDARY BENZYLAMINE INCLUDING (SP(3))C-C(SP(3)) BOND ACTIVATION UNDER MILD CONDITIONS
Vv. Dunina et Eb. Golovan, THE UNPRECEDENTED TRANSFORMATION OF A STERICALLY CROWDED CYCLOPALLADATED SECONDARY BENZYLAMINE INCLUDING (SP(3))C-C(SP(3)) BOND ACTIVATION UNDER MILD CONDITIONS, INORGANIC CHEMISTRY COMMUNICATIONS, 1(1), 1998, pp. 12-14
An unusual process of palladium mediated cleavage of an (sp(3))C-C(sp(
3)) bond between two non-activated carbon atoms in a sterically crowde
d secondary benzylamine is discovered. It includes the conversion of c
yclopalladated N-methyl-alpha-tert-butplbenzylamine formed at the firs
t stage into the ortho-palladated N-methylbenzylidenamine. (C) 1998 El
sevier Science S.A.