A convenient one-pot system has been developed, allowing the synthesis of highly substituted dihydropyridines via a C–H activation/6π-electrocyclization pathway. The reaction proceeds with high regioselectivity, and we disclose the first example of isolated dihydropyridines lacking substitution in the 2 position. Moreover, the use of a simple well-defined low-valent cobalt complex without the need for reducing agents or additives in combination with computational studies provides a clearer insight into the C–H activation pathway than was previously reported
The study and application of transition metal hydrides (TMH) has been an active area of chemical res...
A regioselective synthesis of polycyclic substituted pyridines is reported. Key step is the cobalt-...
We report a Rh(I)-catalyzed C–H activation/alkenylation/electrocyclization cascade and subsequent r...
A convenient one-pot system has been developed, allowing the synthesis of highly substituted dihydro...
The development of a first row transition metal (cobalt)-based catalyst for the as yet unexplored C–...
A versatile reaction cascade leading to highly substituted 1,2,3,6-tetrahydropyridines has been deve...
Transition metal-catalyzed C–H activation has become a powerful approach for atom- and step-economic...
The phosphine-catalyzed synthesis of 1,2-dihydropyridines via an alkyne isomerization/electrocycliza...
A cobalt–triarylphosphine catalyst promotes an annulation reaction of an α,β-unsaturated imine and a...
ABSTRACT: We describe a cobalt-catalyzed hydroacylation of 1,3-dienes with non-chelating aldehydes. ...
A facile C–H activation and functionalization of aromatic imines is presented using low-valent cobal...
In this thesis, I describe chelation-assisted cobalt-catalyzed insertion of C–C multiple bond into C...
A convenient one-pot C-H alkenylation/electrocyclization/aromatization sequence has been developed f...
As an earth-abundant first-row transition metal, cobalt catalysts offer a broad range of economical ...
Electrochemical oxidative C–H/N–H activations have been accomplished with a versatile cobalt catalys...
The study and application of transition metal hydrides (TMH) has been an active area of chemical res...
A regioselective synthesis of polycyclic substituted pyridines is reported. Key step is the cobalt-...
We report a Rh(I)-catalyzed C–H activation/alkenylation/electrocyclization cascade and subsequent r...
A convenient one-pot system has been developed, allowing the synthesis of highly substituted dihydro...
The development of a first row transition metal (cobalt)-based catalyst for the as yet unexplored C–...
A versatile reaction cascade leading to highly substituted 1,2,3,6-tetrahydropyridines has been deve...
Transition metal-catalyzed C–H activation has become a powerful approach for atom- and step-economic...
The phosphine-catalyzed synthesis of 1,2-dihydropyridines via an alkyne isomerization/electrocycliza...
A cobalt–triarylphosphine catalyst promotes an annulation reaction of an α,β-unsaturated imine and a...
ABSTRACT: We describe a cobalt-catalyzed hydroacylation of 1,3-dienes with non-chelating aldehydes. ...
A facile C–H activation and functionalization of aromatic imines is presented using low-valent cobal...
In this thesis, I describe chelation-assisted cobalt-catalyzed insertion of C–C multiple bond into C...
A convenient one-pot C-H alkenylation/electrocyclization/aromatization sequence has been developed f...
As an earth-abundant first-row transition metal, cobalt catalysts offer a broad range of economical ...
Electrochemical oxidative C–H/N–H activations have been accomplished with a versatile cobalt catalys...
The study and application of transition metal hydrides (TMH) has been an active area of chemical res...
A regioselective synthesis of polycyclic substituted pyridines is reported. Key step is the cobalt-...
We report a Rh(I)-catalyzed C–H activation/alkenylation/electrocyclization cascade and subsequent r...