Nickel phthalocyanine with polyethylene glycol- 400 is described as a reusable green catalytic system for highly chemo- and regioselective reduction of carbonyl compounds to corresponding alcohols at room temperature. The catalytic system showed wide substrate scope covering aromatic, hetero aromatic and aliphatic carbonyl compounds with high turnover number and frequency. In the present study, 1,3- and 1,4-benzenedicarbaldehydes have been regioselectively reduced to corresponding alcohols for the first time. The catalyst was reused up to seven times without any significance loss in activity
A new method for synthesizing ortho-substituted benzamides has been developed through the nickel-med...
Simple and commercially available metal amides are investigated as catalysts for the chemical depoly...
Simple and commercially available metal amides are investigated as catalysts for the chemical depoly...
Zinc phthalocyanine with PEG-400 was established as a catalytic system for chemo and regioselective ...
Green is the future of chemistry. Catalysts with high selectivity are the key to green chemistry. Po...
The reduction of p-nitrophenol to p-aminophenol has become a benchmark reaction for testing the effi...
The development of asymmetric transition-metal-catalyzed reactions has emerged as an important area ...
Abstract: Iron phthalocyanine with iron sulfate has been successfully applied for high chemo- and ...
Transition metal catalyzed cross-coupling reactions have become a staple of organic synthesis and ar...
A highly regioselective nickel-catalyzed reductive couplings of propargyl alcohol derivatives and al...
A highly regioselective nickel-catalyzed reductive couplings of propargyl alcohol derivatives and al...
In recent years, the Jarvo lab has developed a range of stereospecific nickel-catalyzed Kumada-type ...
Zn(BH4)2/2NaCl, obtained by the reaction of ZnCl2 and NaBH4 ,is a stable, efficient and selective re...
We report a strategy for the catalytic conversion of lignosulfonate into phenols over heterogeneous ...
© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, WeinheimA catalytic [2+2+2] cyclotrimerization of unactivat...
A new method for synthesizing ortho-substituted benzamides has been developed through the nickel-med...
Simple and commercially available metal amides are investigated as catalysts for the chemical depoly...
Simple and commercially available metal amides are investigated as catalysts for the chemical depoly...
Zinc phthalocyanine with PEG-400 was established as a catalytic system for chemo and regioselective ...
Green is the future of chemistry. Catalysts with high selectivity are the key to green chemistry. Po...
The reduction of p-nitrophenol to p-aminophenol has become a benchmark reaction for testing the effi...
The development of asymmetric transition-metal-catalyzed reactions has emerged as an important area ...
Abstract: Iron phthalocyanine with iron sulfate has been successfully applied for high chemo- and ...
Transition metal catalyzed cross-coupling reactions have become a staple of organic synthesis and ar...
A highly regioselective nickel-catalyzed reductive couplings of propargyl alcohol derivatives and al...
A highly regioselective nickel-catalyzed reductive couplings of propargyl alcohol derivatives and al...
In recent years, the Jarvo lab has developed a range of stereospecific nickel-catalyzed Kumada-type ...
Zn(BH4)2/2NaCl, obtained by the reaction of ZnCl2 and NaBH4 ,is a stable, efficient and selective re...
We report a strategy for the catalytic conversion of lignosulfonate into phenols over heterogeneous ...
© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, WeinheimA catalytic [2+2+2] cyclotrimerization of unactivat...
A new method for synthesizing ortho-substituted benzamides has been developed through the nickel-med...
Simple and commercially available metal amides are investigated as catalysts for the chemical depoly...
Simple and commercially available metal amides are investigated as catalysts for the chemical depoly...