A nitrile-based template attached with a phenylacetic acid framework promoted meta-selective C–H bond olefination. This palladium-catalyzed protocol is applicable to a wide range of substituted phenylacetic acids and tolerates a variety of functional groups. The versatility of this operationally simple method has been demonstrated through drug diversification
Selective meta-C–H activation of arenes to date has met with a limited number of functionalizations....
Palladium catalyzed selective distal C-H activation with nitrile based templates has been of signifi...
To expand the scope of meta-functionalization, a pyrimidine-based template effective for the formati...
A nitrile-based template attached with a phenylacetic acid framework promoted meta-selective C–H bon...
A nitrile-based template attached with a phenylacetic acid framework promoted meta-selective CH bond...
A nitrile-based template attached with a phenylacetic acid framework promoted <i>meta</i>-selective ...
Herein, we present m-C-H olefination on derivatives of phenylacetic acids by tethering with a simple...
Palladium-catalyzed coupling between aryl halides and alkenes (Mizoroki–Heck reaction) is one of the...
The remote meta-selective C-H bond functionalization of aromatic compounds is one of the most challe...
This discovery illustrates selective meta C-H bond activation from multiple non-equivalent C-H bonds...
Strong σ-coordination by a heteroatom containing Directing Group (DG) is one of the effective s...
This article describes the development of a new aliphatic nitrile-template-directed remote meta-sele...
The palladium-catalyzed meta-olefination of arene-tethered diols attached to a well-designed pyrimid...
Divinylbenzene derivatives represent an important class of molecular building blocks in organic chem...
Palladium-catalyzed coupling between aryl halides and alkenes (Mizoroki-Heck reaction) is one of the...
Selective meta-C–H activation of arenes to date has met with a limited number of functionalizations....
Palladium catalyzed selective distal C-H activation with nitrile based templates has been of signifi...
To expand the scope of meta-functionalization, a pyrimidine-based template effective for the formati...
A nitrile-based template attached with a phenylacetic acid framework promoted meta-selective C–H bon...
A nitrile-based template attached with a phenylacetic acid framework promoted meta-selective CH bond...
A nitrile-based template attached with a phenylacetic acid framework promoted <i>meta</i>-selective ...
Herein, we present m-C-H olefination on derivatives of phenylacetic acids by tethering with a simple...
Palladium-catalyzed coupling between aryl halides and alkenes (Mizoroki–Heck reaction) is one of the...
The remote meta-selective C-H bond functionalization of aromatic compounds is one of the most challe...
This discovery illustrates selective meta C-H bond activation from multiple non-equivalent C-H bonds...
Strong σ-coordination by a heteroatom containing Directing Group (DG) is one of the effective s...
This article describes the development of a new aliphatic nitrile-template-directed remote meta-sele...
The palladium-catalyzed meta-olefination of arene-tethered diols attached to a well-designed pyrimid...
Divinylbenzene derivatives represent an important class of molecular building blocks in organic chem...
Palladium-catalyzed coupling between aryl halides and alkenes (Mizoroki-Heck reaction) is one of the...
Selective meta-C–H activation of arenes to date has met with a limited number of functionalizations....
Palladium catalyzed selective distal C-H activation with nitrile based templates has been of signifi...
To expand the scope of meta-functionalization, a pyrimidine-based template effective for the formati...