Although the catalytic carboxylation of unactivated alkyl electrophiles has reached remarkable levels of sophistication, the intermediacy of (phenanthroline)Ni(I)–alkyl species—complexes proposed in numerous Ni-catalyzed reductive cross-coupling reactions—has been subject to speculation. Herein we report the synthesis of such elusive (phenanthroline)Ni(I) species and their reactivity with CO2, allowing us to address a long-standing question related to Ni-catalyzed carboxylation reactions
In recent years a significant progress has been made for the carboxylation of aryl and benzyl hal...
Nickel-catalyzed cross-coupling reactions have become a powerful methodology to construct C-heteroat...
Detailed kinetic studies of the reaction of a model Ni-0 complex with a range of aryl electrophiles ...
The authors acknowledge the ERC (Advanced Researcher award-FUNCAT, CO2Chem) and King Saud University...
The first part of this thesis deals with a mechanistic investigation into the conversion of the know...
Nickel-catalyzed reductive carboxylation reactions of aryl electrophiles typically require the use o...
The authors acknowledge FAPERJ for providing research grants and financial support. MB thanks the Sc...
Olefins devoid of directing or activating groups have been dicarbofunctionalized here with two elect...
A deceptively simple proton abstraction from nickel-bound formate not only prepares the resulting CO...
The nickel-catalyzed carboxylation of organic halides or pseudohalides using carbon dioxide is an em...
The recent years have witnessed the development of metal-catalyzed reductive carboxylation of organi...
University of Minnesota Ph.D. dissertation.June 2018. Major: Chemistry. Advisor: Connie Lu. 1 compu...
Detailed kinetic studies of the reaction of a model Ni0 complex with a range of aryl electrophiles h...
Recent advances in heterobimetallic chemistry have revealed the potential for mixed-metal systems to...
Inert C−O bond activation has been an important research area because ethers have the potential to r...
In recent years a significant progress has been made for the carboxylation of aryl and benzyl hal...
Nickel-catalyzed cross-coupling reactions have become a powerful methodology to construct C-heteroat...
Detailed kinetic studies of the reaction of a model Ni-0 complex with a range of aryl electrophiles ...
The authors acknowledge the ERC (Advanced Researcher award-FUNCAT, CO2Chem) and King Saud University...
The first part of this thesis deals with a mechanistic investigation into the conversion of the know...
Nickel-catalyzed reductive carboxylation reactions of aryl electrophiles typically require the use o...
The authors acknowledge FAPERJ for providing research grants and financial support. MB thanks the Sc...
Olefins devoid of directing or activating groups have been dicarbofunctionalized here with two elect...
A deceptively simple proton abstraction from nickel-bound formate not only prepares the resulting CO...
The nickel-catalyzed carboxylation of organic halides or pseudohalides using carbon dioxide is an em...
The recent years have witnessed the development of metal-catalyzed reductive carboxylation of organi...
University of Minnesota Ph.D. dissertation.June 2018. Major: Chemistry. Advisor: Connie Lu. 1 compu...
Detailed kinetic studies of the reaction of a model Ni0 complex with a range of aryl electrophiles h...
Recent advances in heterobimetallic chemistry have revealed the potential for mixed-metal systems to...
Inert C−O bond activation has been an important research area because ethers have the potential to r...
In recent years a significant progress has been made for the carboxylation of aryl and benzyl hal...
Nickel-catalyzed cross-coupling reactions have become a powerful methodology to construct C-heteroat...
Detailed kinetic studies of the reaction of a model Ni-0 complex with a range of aryl electrophiles ...