A catalytic protocol for the preparation of α,α-difluoro-β-alkyl-β-ketoamides is developed employing a Pd-mediated carbonylative Suzuki coupling between alkylboron reagents and bromodifluoroacetamides with COgen as the CO source. The reaction reveals good functional group tolerance providing a broad selection of α,α-difluoro-β-alkyl-β-ketoamides in moderate to good yields, which represent useful precursors for further synthetic manipulation. Finally, the methodology is amenable to <sup>13</sup>C-isotope labeling at the ketone carbon applying <sup>13</sup>C-COgen
The direct carbonylative palladium catalyzed synthesis of monoprotected 1,3-ketoaldehydes is reporte...
The carbonylation of carbenes through catalytic cycles is highly desirable due to the importance of ...
Carbon monoxide (CO) represents an important C1-building block for the construction of some of the m...
A palladium-catalyzed carbonylative approach for the direct conversion of (hetero)aryl bromides into...
A simple method for accessing perfluoroalkyl-substituted enones is described applying a four-compone...
We report on a three-component palladium-catalyzed coupling strategy for accessing a wide range of 1...
International audienceThe Suzuki-Miyaura cross-coupling is one of the most useful synthetic tools to...
A versatile palladium-catalyzed double carbonylation of aryl bromides has been developed. Using Pd(O...
A novel and highly selective methodology based on palladium catalyzed cross coupling of either α-hal...
Palladium-catalyzed carbonylative coupling reactions of various N,N-bis(methanesulfonyl)amides with ...
An efficient and general protocol for the synthesis of α,β-unsaturated aldehydes, esters, and amides...
ABSTRACT: The carbonylative Suzuki−Miyaura reaction between aryl bromides and arylboronic acid equiv...
Alkyl aryl ketones were synthesized by the carbonylative cross-coupling reaction of alkyl iodides an...
A palladium-catalyzed perfluoroalkylative carbonylation of 2-allylaryl trifluoromethanesulfonates ha...
Functionalizations of aryl and heteroaryl halides as well as of haloketones are of major importance ...
The direct carbonylative palladium catalyzed synthesis of monoprotected 1,3-ketoaldehydes is reporte...
The carbonylation of carbenes through catalytic cycles is highly desirable due to the importance of ...
Carbon monoxide (CO) represents an important C1-building block for the construction of some of the m...
A palladium-catalyzed carbonylative approach for the direct conversion of (hetero)aryl bromides into...
A simple method for accessing perfluoroalkyl-substituted enones is described applying a four-compone...
We report on a three-component palladium-catalyzed coupling strategy for accessing a wide range of 1...
International audienceThe Suzuki-Miyaura cross-coupling is one of the most useful synthetic tools to...
A versatile palladium-catalyzed double carbonylation of aryl bromides has been developed. Using Pd(O...
A novel and highly selective methodology based on palladium catalyzed cross coupling of either α-hal...
Palladium-catalyzed carbonylative coupling reactions of various N,N-bis(methanesulfonyl)amides with ...
An efficient and general protocol for the synthesis of α,β-unsaturated aldehydes, esters, and amides...
ABSTRACT: The carbonylative Suzuki−Miyaura reaction between aryl bromides and arylboronic acid equiv...
Alkyl aryl ketones were synthesized by the carbonylative cross-coupling reaction of alkyl iodides an...
A palladium-catalyzed perfluoroalkylative carbonylation of 2-allylaryl trifluoromethanesulfonates ha...
Functionalizations of aryl and heteroaryl halides as well as of haloketones are of major importance ...
The direct carbonylative palladium catalyzed synthesis of monoprotected 1,3-ketoaldehydes is reporte...
The carbonylation of carbenes through catalytic cycles is highly desirable due to the importance of ...
Carbon monoxide (CO) represents an important C1-building block for the construction of some of the m...