An efficient, scalable, atom-economical, regio-selective air stable Cp*Co(iii) catalyzed C-H and C-O coupling via a C-H activation/oxygen atom transfer reaction of quinoline N-oxide and an internal alkyne is reported. Such a catalytic transformation is witnessed for the first time with a cobalt catalyst and using N-oxide as a traceless directing group, in contrast to the existing literature. The developed synthetic methodology is straightforward and possesses various functional group tolerances, including heterocycles.
An efficient and external oxidant-free, Cp*Co(III) -catalyzed C(sp(3) )-H bond amidation of 8-methylquinoline, using oxazolone as an efficient amidating agent, is reported for the first time under mild conditions. The reaction is selective and tolerates a variety of functional groups. Based on previous reports and experimental results, the deprotonation pathway proceeds through an external base-assisted concerted metalation and deprotonation process.
Efficient, scalable cobalt-catalyzed redox-neutral [4+2] annulation of readily available oximes and alkyne is reported. The developed synthetic methodology is widely applicable and tolerates various functional groups including heterocycles. A stable Cp*Co(III) neutral complex is employed as the catalyst for this redox-neutral [4+2] annulation reaction, which progresses smoothly by way of a reversible cyclometallation without any external oxidizing agent, and produces only water as the side product.
Efficient,
atom-economical, highly regioselective C(sp3)–H
bond alkenylation of 8-methylquinoline catalyzed by (Cp*)Co(III)
is reported. A well-defined, air-stable, molecular cobalt catalyst,
Cp*Co(III), is employed for the first time in C(sp3)–H
bond activation. The developed methodology is broadly applicable and
tolerates a variety of functional groups, under mild conditions. Experimental
and density functional theory (DFT) results suggest that the initial
cyclometalation was occurred via an external-base-assisted concerted
metalation deprotonation pathway.
Efficient, sustainable, highly regiospecific substituted pyrroles were synthesized using a well-defined, air stable, molecular iron(0) complex. The developed methodology is broadly applicable and tolerates a variety of functional groups. C-2, C-3, and C-2 & C-4 substituted pyrroles were synthesized in good yield. Symmetrical bis-pyrroles were accessible for the first time using an iron catalyst. On the basis of the experimental observation, we propose that the reaction proceeds through a hydrogen autotransfer process followed by second oxidation/intramolecular dehydrative condensation to provide the pyrrole.
Cp*Co -catalyzed highly regioselective mono- and bis-annulation of arylamides with 1,3-diynes using N-OMe as an internal oxidant is demonstrated. This atom-economical transformation does not require any external oxidant and tolerates many functional groups. Various symmetrical and unsymmetrical heterocycles (homo and hetero) are accessed with predictable regio- and chemoselectivity.
An efficient, unprecedented reactivity of Cp*Co(III) for the synthesis of tetrasubstituted allenes under mild conditions is disclosed. Electron-rich and highly nucleophilic cobalt facilitates the dehydrative C-H bond allenylation directly from propargylic alcohols without any derivatization. The reaction proceeds via reversible cyclometalation followed by alcohol-directed regioselective alkyne insertion and β-hydroxy elimination to provide the tetrasubstituted allenes.
A general and efficient procedure for C-H alkenylation of arenes with a broad substrate scope catalyzed by Cp*Co was demonstrated with alkynes. A highly selective mono-alkenylation and sequential bis-C-H bond functionalization was displayed to exemplify the versatility of the cobalt catalyst. Isolation of cationic Cp*Co -alkenyl intermediate was achieved under identical catalytic conditions to further establish the proposed pathway.
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