To expand the scope of meta-functionalization, a pyrimidine-based template effective for the formation of beta-aryl aldehydes and ketones, using allyl alcohols, by meta-C-H activation of benzylsulfonyl esters is described. In addition, a, b-unsaturated aldehydes were generated by in situ olefination and deprotection of allyl benzyl ethers. These new functionalizations at the meta-position of an arene have also been successfully implemented in benzylphosphonate, phenethyl carbonyl, and phenethylsulfonyl ester scaffolds. Key to these successful new functionalizations is the creation of an electropositive palladium center by accepting the electron cloud from the metal to the energetically low-lying p-orbitals of pyrimidine ring, and it favors ...
Site-selective C-H functionalization has emerged as an efficient tool in simplifying the synthesis o...
Divinylbenzene derivatives represent an important class of molecular building blocks in organic chem...
A catalytic meta-selective C-H functionalization of 2-phenylpyridines using a range of tertiary hali...
Development of meta-C-H functionalization reactions at room temperature continues to be a tough chal...
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 meta-selective C–H bon...
Selective meta-C-H activation of arenes to date has met with a limited number of functionalizations....
This article describes the development of a new aliphatic nitrile-template-directed remote meta-sele...
The remote meta-selective C-H bond functionalization of aromatic compounds is one of the most challe...
The palladium-catalyzed meta-olefination of arene-tethered diols attached to a well-designed pyrimid...
Site selective C-H bond activation/C-C bond formation is an ideal target for organic chemists owing ...
Herein, we present m-C-H olefination on derivatives of phenylacetic acids by tethering with a simple...
The selective formation of new carbon-carbon bonds is a central challenge for organic synthesis; org...
The use of a template as a linchpin motif in directed remote C–H functionalization is a versatile ye...
Rhodium-catalyzed ortho-C-H functionalization is well known in the literature. Described herein is t...
Site-selective C-H functionalization has emerged as an efficient tool in simplifying the synthesis o...
Divinylbenzene derivatives represent an important class of molecular building blocks in organic chem...
A catalytic meta-selective C-H functionalization of 2-phenylpyridines using a range of tertiary hali...
Development of meta-C-H functionalization reactions at room temperature continues to be a tough chal...
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 meta-selective C–H bon...
Selective meta-C-H activation of arenes to date has met with a limited number of functionalizations....
This article describes the development of a new aliphatic nitrile-template-directed remote meta-sele...
The remote meta-selective C-H bond functionalization of aromatic compounds is one of the most challe...
The palladium-catalyzed meta-olefination of arene-tethered diols attached to a well-designed pyrimid...
Site selective C-H bond activation/C-C bond formation is an ideal target for organic chemists owing ...
Herein, we present m-C-H olefination on derivatives of phenylacetic acids by tethering with a simple...
The selective formation of new carbon-carbon bonds is a central challenge for organic synthesis; org...
The use of a template as a linchpin motif in directed remote C–H functionalization is a versatile ye...
Rhodium-catalyzed ortho-C-H functionalization is well known in the literature. Described herein is t...
Site-selective C-H functionalization has emerged as an efficient tool in simplifying the synthesis o...
Divinylbenzene derivatives represent an important class of molecular building blocks in organic chem...
A catalytic meta-selective C-H functionalization of 2-phenylpyridines using a range of tertiary hali...