A novel palladium-catalyzed carbonylation of indoles with CO and aromatic boronic acids for the synthesis of indol-3-yl aryl ketones was developed. The reaction tolerates a wide range of functional groups and gives a variety of valuable indol-3-yl aryl ketones in high yields under mild conditions
A novel synthesis of indoles having electron withdrawing substituents in the 3-position has been dev...
The palladium catalyzed reductive cyclization of substituted ortho-nitrostyrenes is a powerful metho...
Functionalizations of aryl and heteroaryl halides as well as of haloketones are of major importance ...
A novel strategy involving a first oxidative iodination and subsequent Pd<sup>0</sup>-catalyzed carb...
A novel strategy involving a first oxidative iodination and subsequent Pd<sup>0</sup>-catalyzed carb...
A novel strategy involving a first oxidative iodination and subsequent Pd<sup>0</sup>-catalyzed carb...
A novel palladium catalyzed approach to 3-arylindoles was developed from indoles and cyclohexanones....
A general method for regioselective C3-benzylation of indoles has been developed. Various 3-substitu...
An efficient synthesis of indolizine derivatives by palladium-catalyzed oxidative carbonylation of p...
Palladium-catalyzed synthesis of indoles by cyclization of beta-nitrostyrenes using carbon monoxide ...
A palladium-catalyzed approach to intermolecular carbonylative C–H functionalization is described. T...
A Pd-catalyzed carbonylative dearomatization via an acyl Pd complex has been developed. Diversified ...
University Honors Capstone Project Paper, University of Minnesota Duluth, 2015.The indole scaffold p...
A Pd-catalyzed carbonylative dearomatization via an acyl Pd complex has been developed. Diversified ...
A novel synthesis of indoles having electron withdrawing substituents in the 3-position has been dev...
A novel synthesis of indoles having electron withdrawing substituents in the 3-position has been dev...
The palladium catalyzed reductive cyclization of substituted ortho-nitrostyrenes is a powerful metho...
Functionalizations of aryl and heteroaryl halides as well as of haloketones are of major importance ...
A novel strategy involving a first oxidative iodination and subsequent Pd<sup>0</sup>-catalyzed carb...
A novel strategy involving a first oxidative iodination and subsequent Pd<sup>0</sup>-catalyzed carb...
A novel strategy involving a first oxidative iodination and subsequent Pd<sup>0</sup>-catalyzed carb...
A novel palladium catalyzed approach to 3-arylindoles was developed from indoles and cyclohexanones....
A general method for regioselective C3-benzylation of indoles has been developed. Various 3-substitu...
An efficient synthesis of indolizine derivatives by palladium-catalyzed oxidative carbonylation of p...
Palladium-catalyzed synthesis of indoles by cyclization of beta-nitrostyrenes using carbon monoxide ...
A palladium-catalyzed approach to intermolecular carbonylative C–H functionalization is described. T...
A Pd-catalyzed carbonylative dearomatization via an acyl Pd complex has been developed. Diversified ...
University Honors Capstone Project Paper, University of Minnesota Duluth, 2015.The indole scaffold p...
A Pd-catalyzed carbonylative dearomatization via an acyl Pd complex has been developed. Diversified ...
A novel synthesis of indoles having electron withdrawing substituents in the 3-position has been dev...
A novel synthesis of indoles having electron withdrawing substituents in the 3-position has been dev...
The palladium catalyzed reductive cyclization of substituted ortho-nitrostyrenes is a powerful metho...
Functionalizations of aryl and heteroaryl halides as well as of haloketones are of major importance ...