Unknown

Dataset Information

0

Activation of sp3 C-H bonds with cobalt(I): catalytic synthesis of enamines.


ABSTRACT: C-H bond activation has been extensively studied with (Cp*)M(L)n (M = Ir, Rh), but cobalt, the third member of this triad, has not previously been shown to activate sp3 C-H bonds. Further, practical functionalization of the metal alkyl products of oxidative addition has not been fully explored. Toward these ends, we have developed catalytic dehydrogenation of alkyl amines with a Co(I) catalyst. Amine substrates are protected with vinyl silanes, followed by catalytic transfer hydrogenation, to yield a broad range of stable protected enamines and 1,2-diheteroatom-substituted alkenes, including several unprecedented heterocycles. (Cp*)Co(VTMS)2 catalyzes transfer hydrogenation under surprisingly mild conditions with high chemo-, regio-, and diastereoselectivity, while tolerating additional functionality.

SUBMITTER: Bolig AD 

PROVIDER: S-EPMC2536615 | biostudies-literature | 2007 Nov

REPOSITORIES: biostudies-literature

altmetric image

Publications

Activation of sp3 C-H bonds with cobalt(I): catalytic synthesis of enamines.

Bolig Andrew D AD   Brookhart Maurice M  

Journal of the American Chemical Society 20071107 47


C-H bond activation has been extensively studied with (Cp*)M(L)n (M = Ir, Rh), but cobalt, the third member of this triad, has not previously been shown to activate sp3 C-H bonds. Further, practical functionalization of the metal alkyl products of oxidative addition has not been fully explored. Toward these ends, we have developed catalytic dehydrogenation of alkyl amines with a Co(I) catalyst. Amine substrates are protected with vinyl silanes, followed by catalytic transfer hydrogenation, to yi  ...[more]

Similar Datasets

| S-EPMC5813831 | biostudies-literature
| S-EPMC6339699 | biostudies-literature
| S-EPMC5502808 | biostudies-literature
| S-EPMC2841429 | biostudies-literature
| S-EPMC6880961 | biostudies-literature
| S-EPMC7842137 | biostudies-literature
| S-EPMC9401092 | biostudies-literature
| S-EPMC6383370 | biostudies-literature
| S-EPMC2794962 | biostudies-literature
| S-EPMC2727875 | biostudies-literature