An efficient C–H activation method for the <i>ortho</i> alkynylation of aromatic <i>N-</i>methoxyamides with hypervalent iodine–alkyne reagent using a ruthenium catalyst is described. The reaction proceeds under mild reaction conditions with broad substrate scope. A possible catalytic cycle involving a ruthenium carboxylate assisted C–H bond cleavage is proposed from the preliminary mechanistic evidence
Molecular ruthenium catalysts are now currently used to perform selective carbon– carbon bond format...
The alkynylation of naphthols takes place with total regiocontrol at the <i>peri</i> position of the...
The cationic ruthenium hydride complex [(PCy3)2(CO)(CH3CN)2RuH]+BF4- was found to be a highly effect...
An efficient C–H activation method for the <i>ortho</i> alkynylation of aromatic <i>N-</i>methoxyami...
The rhodium(III)-catalyzed ortho C[BOND]H alkynylation of non-electronically activated arenes is dis...
A direct, regioselective alkenylation of aromatic C–H bonds of aryl- and heteroarylpyridines and rel...
An efficient Rh(III)- and Ir(III)-catalyzed, chelation-assisted C–H alkynylation of a broad scope ...
C–H alkynylations with weakly coordinating acids were accomplished by the aid of an expedient ruthen...
An efficient Rh(III)- and Ir(III)-catalyzed, chelation-assisted C H alkynylation of a broad scope of...
The Rh(III)-catalyzed ortho-alkynylation of benzaldehydes is enabled by the transient formation of a...
Versatile ruthenium catalysts enabled unprecedented C–H bond oxygenations of aryl Weinreb amides wit...
The ruthenium-catalyzed hydroarylation of alkynes with benzamides proceeds regio- and stereoselectiv...
A highly selective ruthenium-catalyzed C-H activation/annulation of alkyne-tethered N-alkoxybenzamid...
The ruthenium-catalyzed coupling reactions of benzamides with alkynes in the presence of acetic acid...
The alkynylation of naphthols takes place with total regiocontrol at the peri position of the hydrox...
Molecular ruthenium catalysts are now currently used to perform selective carbon– carbon bond format...
The alkynylation of naphthols takes place with total regiocontrol at the <i>peri</i> position of the...
The cationic ruthenium hydride complex [(PCy3)2(CO)(CH3CN)2RuH]+BF4- was found to be a highly effect...
An efficient C–H activation method for the <i>ortho</i> alkynylation of aromatic <i>N-</i>methoxyami...
The rhodium(III)-catalyzed ortho C[BOND]H alkynylation of non-electronically activated arenes is dis...
A direct, regioselective alkenylation of aromatic C–H bonds of aryl- and heteroarylpyridines and rel...
An efficient Rh(III)- and Ir(III)-catalyzed, chelation-assisted C–H alkynylation of a broad scope ...
C–H alkynylations with weakly coordinating acids were accomplished by the aid of an expedient ruthen...
An efficient Rh(III)- and Ir(III)-catalyzed, chelation-assisted C H alkynylation of a broad scope of...
The Rh(III)-catalyzed ortho-alkynylation of benzaldehydes is enabled by the transient formation of a...
Versatile ruthenium catalysts enabled unprecedented C–H bond oxygenations of aryl Weinreb amides wit...
The ruthenium-catalyzed hydroarylation of alkynes with benzamides proceeds regio- and stereoselectiv...
A highly selective ruthenium-catalyzed C-H activation/annulation of alkyne-tethered N-alkoxybenzamid...
The ruthenium-catalyzed coupling reactions of benzamides with alkynes in the presence of acetic acid...
The alkynylation of naphthols takes place with total regiocontrol at the peri position of the hydrox...
Molecular ruthenium catalysts are now currently used to perform selective carbon– carbon bond format...
The alkynylation of naphthols takes place with total regiocontrol at the <i>peri</i> position of the...
The cationic ruthenium hydride complex [(PCy3)2(CO)(CH3CN)2RuH]+BF4- was found to be a highly effect...