Disclosed is a new, catalytic, and general methodology for the chemical synthesis of biaryl, heterobiaryl, and polyaryl molecules by the cross-coupling of <i>o</i>-methoxybenzamides with aryl boroneopentylates. The reaction is based on the activation of the unreactive C–OMe bond by the proximate amide directing group using catalytic RuH<sub>2</sub>(CO)(PPh<sub>3</sub>)<sub>3</sub> conditions. A one-step, base-free coupling process is thereby established that has the potential to supersede the useful two-step directed <i>ortho</i> metalation/cross-coupling reaction involving cryogenic temperature and strong base conditions. High regioselectivity, orthogonality with the Suzuki–Miyaura reaction, operational simplicity, minimum waste, and...
The use of bis-boronic acid for the direct synthesis of boronic acids has greatly facilitated the tw...
A method for the synthesis of biaryls and heterobiaryls from arenes and haloarenes without the inter...
The biaryl core has been identified by medicinal chemists as a privileged structure in pharmaceutica...
A new, catalytic, and general methodology for the synthesis of biaryls and heterobiaryls by the cros...
A new and general synthetic methodology for the construction of biaryl, heterobiaryl, and polyaryl m...
International audienceA general synthesis of stable ortho-boropinacolato aryl and heteroaryl sulfona...
International audienceA general synthesis of stable ortho-boropinacolato aryl and heteroaryl sulfona...
We report an efficient palladium-catalyzed <i>ortho</i>–C-H arylation of acetophenone oxime ethers w...
We disclose a general method for selective ortho-C–H arylation of cyclic and <i>N</i>,<i>N</i>-dialk...
The development of a Pd-catalyzed oxidative <i>ortho</i>-C–H borylation with <i>N</i>-arylbenzamides...
Catalytic carbon-carbon bond formation based on cross-coupling reactions plays a central role in the...
Catalytic carbon-carbon bond formation based on cross-coupling reactions plays a central role in the...
Catalytic carbon-carbon bond formation based on cross-coupling reactions plays a central role in the...
Catalytic carbon-carbon bond formation based on cross-coupling reactions plays a central role in the...
Organotrifluoroborates have emerged in the past decade as suitable nucleophilic partners for the Suz...
The use of bis-boronic acid for the direct synthesis of boronic acids has greatly facilitated the tw...
A method for the synthesis of biaryls and heterobiaryls from arenes and haloarenes without the inter...
The biaryl core has been identified by medicinal chemists as a privileged structure in pharmaceutica...
A new, catalytic, and general methodology for the synthesis of biaryls and heterobiaryls by the cros...
A new and general synthetic methodology for the construction of biaryl, heterobiaryl, and polyaryl m...
International audienceA general synthesis of stable ortho-boropinacolato aryl and heteroaryl sulfona...
International audienceA general synthesis of stable ortho-boropinacolato aryl and heteroaryl sulfona...
We report an efficient palladium-catalyzed <i>ortho</i>–C-H arylation of acetophenone oxime ethers w...
We disclose a general method for selective ortho-C–H arylation of cyclic and <i>N</i>,<i>N</i>-dialk...
The development of a Pd-catalyzed oxidative <i>ortho</i>-C–H borylation with <i>N</i>-arylbenzamides...
Catalytic carbon-carbon bond formation based on cross-coupling reactions plays a central role in the...
Catalytic carbon-carbon bond formation based on cross-coupling reactions plays a central role in the...
Catalytic carbon-carbon bond formation based on cross-coupling reactions plays a central role in the...
Catalytic carbon-carbon bond formation based on cross-coupling reactions plays a central role in the...
Organotrifluoroborates have emerged in the past decade as suitable nucleophilic partners for the Suz...
The use of bis-boronic acid for the direct synthesis of boronic acids has greatly facilitated the tw...
A method for the synthesis of biaryls and heterobiaryls from arenes and haloarenes without the inter...
The biaryl core has been identified by medicinal chemists as a privileged structure in pharmaceutica...