Herein, we present m-C-H olefination on derivatives of phenylacetic acids by tethering with a simple nitrile-based template through palladium catalysis. Notably, the versatility of the method is evaluated with a wide range of phenylacetic acid derivatives for obtaining the meta-olefination products in fair to excellent yields with outstanding selectivities under mild conditions. Significantly, the present strategy is successfully exemplified for the synthesis of drugs/natural product analogues (naproxen, ibuprofen, paracetamol, and cholesterol). © 2021 American Chemical Society
Palladium-catalysed coupling reactions have been embraced by synthetic chemists as one of the prefer...
Palladium-catalyzed direct lactonization of 2-arylacetic acids through a reaction sequence that incl...
La fonctionnalisation directe des liaisons C-H représente une avancée considérable dans la re...
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 ...
Palladium-catalyzed coupling between aryl halides and alkenes (Mizoroki-Heck reaction) is one of the...
This article describes the development of a new aliphatic nitrile-template-directed remote meta-sele...
Palladium-catalyzed coupling between aryl halides and alkenes (Mizoroki–Heck reaction) is one of the...
Palladium catalyzed selective distal C-H activation with nitrile based templates has been of signifi...
The palladium-catalyzed meta-olefination of arene-tethered diols attached to a well-designed pyrimid...
A novel traceless protecting strategy is presented for the long-standing challenge of conducting the...
Metal-catalyzed cross-coupling reactions to form C-C bonds are a mainstay in the preparation of smal...
This discovery illustrates selective meta C-H bond activation from multiple non-equivalent C-H bonds...
To expand the scope of meta-functionalization, a pyrimidine-based template effective for the formati...
Palladium-catalysed coupling reactions have been embraced by synthetic chemists as one of the prefer...
Palladium-catalyzed direct lactonization of 2-arylacetic acids through a reaction sequence that incl...
La fonctionnalisation directe des liaisons C-H représente une avancée considérable dans la re...
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 ...
Palladium-catalyzed coupling between aryl halides and alkenes (Mizoroki-Heck reaction) is one of the...
This article describes the development of a new aliphatic nitrile-template-directed remote meta-sele...
Palladium-catalyzed coupling between aryl halides and alkenes (Mizoroki–Heck reaction) is one of the...
Palladium catalyzed selective distal C-H activation with nitrile based templates has been of signifi...
The palladium-catalyzed meta-olefination of arene-tethered diols attached to a well-designed pyrimid...
A novel traceless protecting strategy is presented for the long-standing challenge of conducting the...
Metal-catalyzed cross-coupling reactions to form C-C bonds are a mainstay in the preparation of smal...
This discovery illustrates selective meta C-H bond activation from multiple non-equivalent C-H bonds...
To expand the scope of meta-functionalization, a pyrimidine-based template effective for the formati...
Palladium-catalysed coupling reactions have been embraced by synthetic chemists as one of the prefer...
Palladium-catalyzed direct lactonization of 2-arylacetic acids through a reaction sequence that incl...
La fonctionnalisation directe des liaisons C-H représente une avancée considérable dans la re...