This discovery illustrates selective meta C-H bond activation from multiple non-equivalent C-H bonds present in medicinally relevant arylethanesulfonic acid and the 2-arylpropanoic acid moiety using weakly coordinating nitrile as a directing group. Transformation of the meta olefinated compounds to important organic molecules has been demonstrated. Efforts were made to obtain mechanistic detail of the meta C-H bond functionalization reaction
This Perspective presents the fundamental principles, the elementary reactions, the initial catalyti...
The functionalization of C-H bonds has created new approaches to preparing organic molecules by enab...
Aromatic C-H functionalization, the exchange of hydrogen atoms which are bound to carbon atoms for f...
A nitrile-based template attached with a phenylacetic acid framework promoted meta-selective CH bond...
A catalytic meta-selective C-H functionalization of 2-phenylpyridines using a range of tertiary hali...
A simple and efficient nitrile-directed meta-C-H olefination, acetoxylation, and iodination of biary...
A nitrile-based template attached with a phenylacetic acid framework promoted meta-selective C–H bon...
Selective meta-C-H activation of arenes to date has met with a limited number of functionalizations....
Activation and functionalization of unactivated sp3 C-H bonds have been demonstrated in complex subs...
phenylpropanoic acid and phenolic derivatives were developed using an easily removable nitrile templ...
Selectively activating the distal inactive C-H bond for functionalization is one of the on-going cha...
Cleavage of a C–S bond of benzyl mercaptan led to formation of a new C–C bond during (Z)-selective a...
This article describes the development of a new aliphatic nitrile-template-directed remote meta-sele...
Herein, we present m-C-H olefination on derivatives of phenylacetic acids by tethering with a simple...
The widespread use of transition-metal-mediated C-H bond activation has altered the field of organic...
This Perspective presents the fundamental principles, the elementary reactions, the initial catalyti...
The functionalization of C-H bonds has created new approaches to preparing organic molecules by enab...
Aromatic C-H functionalization, the exchange of hydrogen atoms which are bound to carbon atoms for f...
A nitrile-based template attached with a phenylacetic acid framework promoted meta-selective CH bond...
A catalytic meta-selective C-H functionalization of 2-phenylpyridines using a range of tertiary hali...
A simple and efficient nitrile-directed meta-C-H olefination, acetoxylation, and iodination of biary...
A nitrile-based template attached with a phenylacetic acid framework promoted meta-selective C–H bon...
Selective meta-C-H activation of arenes to date has met with a limited number of functionalizations....
Activation and functionalization of unactivated sp3 C-H bonds have been demonstrated in complex subs...
phenylpropanoic acid and phenolic derivatives were developed using an easily removable nitrile templ...
Selectively activating the distal inactive C-H bond for functionalization is one of the on-going cha...
Cleavage of a C–S bond of benzyl mercaptan led to formation of a new C–C bond during (Z)-selective a...
This article describes the development of a new aliphatic nitrile-template-directed remote meta-sele...
Herein, we present m-C-H olefination on derivatives of phenylacetic acids by tethering with a simple...
The widespread use of transition-metal-mediated C-H bond activation has altered the field of organic...
This Perspective presents the fundamental principles, the elementary reactions, the initial catalyti...
The functionalization of C-H bonds has created new approaches to preparing organic molecules by enab...
Aromatic C-H functionalization, the exchange of hydrogen atoms which are bound to carbon atoms for f...