International audienceA general synthesis of stable ortho-boropinacolato aryl and heteroaryl sulfonamides by directed ortho-metalation (DoM) and either MeOBPin or i-PrOBpin electrophile quench, 3 → 4, is described. A one-pot metalation–Suzuki cross-coupling procedure for the synthesis of biaryls and heterobiaryls, 3 → 5, and a complementary DoM–Ir-catalyzed boronation sequence (Scheme 6) are delineated
Cyclopalladated compounds derived from the ortho-metalation of benzylic tert-butyl thioethers are ex...
The direct formation of (hetero)biaryls from readily available (hetero)aryl halides under mild react...
The Suzuki–Miyaura cross-coupling reaction is one of the most efficient methods to form new carbon-c...
International audienceA general synthesis of stable ortho-boropinacolato aryl and heteroaryl sulfona...
Disclosed is a new, catalytic, and general methodology for the chemical synthesis of biaryl, hetero...
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...
Catalytic procedures are described for the amine-directed borylation of aliphatic and aromatic terti...
Catalytic procedures are described for the amine-directed borylation of aliphatic and aromatic terti...
Heteroaryl ortho-phenoxyethyl amines have been extensively employed in medicinal chemistry as privil...
Heteroaryl ortho-phenoxyethyl amines have been extensively employed in medicinal chemistry as privil...
The installation of sulfonamide pharmacophores on heterobiaryls has successfully been executed by a ...
Organotrifluoroborates have emerged in the past decade as suitable nucleophilic partners for the Suz...
While the Suzuki coupling has gained paramount importance, the basic set-up of the reaction has rema...
Organotrifluoroborates have emerged in the past decade as suitable nucleophilic partners for the Suz...
Cyclopalladated compounds derived from the ortho-metalation of benzylic tert-butyl thioethers are ex...
The direct formation of (hetero)biaryls from readily available (hetero)aryl halides under mild react...
The Suzuki–Miyaura cross-coupling reaction is one of the most efficient methods to form new carbon-c...
International audienceA general synthesis of stable ortho-boropinacolato aryl and heteroaryl sulfona...
Disclosed is a new, catalytic, and general methodology for the chemical synthesis of biaryl, hetero...
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...
Catalytic procedures are described for the amine-directed borylation of aliphatic and aromatic terti...
Catalytic procedures are described for the amine-directed borylation of aliphatic and aromatic terti...
Heteroaryl ortho-phenoxyethyl amines have been extensively employed in medicinal chemistry as privil...
Heteroaryl ortho-phenoxyethyl amines have been extensively employed in medicinal chemistry as privil...
The installation of sulfonamide pharmacophores on heterobiaryls has successfully been executed by a ...
Organotrifluoroborates have emerged in the past decade as suitable nucleophilic partners for the Suz...
While the Suzuki coupling has gained paramount importance, the basic set-up of the reaction has rema...
Organotrifluoroborates have emerged in the past decade as suitable nucleophilic partners for the Suz...
Cyclopalladated compounds derived from the ortho-metalation of benzylic tert-butyl thioethers are ex...
The direct formation of (hetero)biaryls from readily available (hetero)aryl halides under mild react...
The Suzuki–Miyaura cross-coupling reaction is one of the most efficient methods to form new carbon-c...