A weakly coordinating biorelevant intrinsic directing group (DG) assisted site-selective C–H alkenylation via sequential C–H/C–C bond activation has been accomplished under Ru(II)-catalysis using readily accessible cyclopropyl alcohol as an alkenyl surrogate. Utilization of an intrinsic DG, exclusive regioselectivity, functional group diversity, late-stage natural product and drug mutations are the important practical features
International audienceElectron-rich ruthenium(II) catalysts of type (C5R5)XRuL n are used to perform...
A highly selective and switchable ruthenium-catalyzed <i>ortho</i> C–H alkylation and C–H alkenylati...
Herein we report the regio- and stereoselective synthesis of tetrasubstituted alkenes from N-carbamo...
International audienceThe first use of biologically relevant isoindolinones as weak directing groups...
The ruthenium-catalyzed alkenylation reactions of 2-aminobiphenyls and cumylamine proceed smoothly t...
Alkenes and alcohols are among the most abundant and commonly used organic feedstock in industrial p...
International audienceThe first example of a ruthenium-catalyzed C–H bond alkylation via six-membere...
Cationic ruthenium(II) complexes enabled catalytic twofold C–H bond functionalizations with weakly c...
Organic syntheses based on the activation of C–H bonds catalysed by transition metals (TM) are of gr...
Carboxylate assistance enabled efficient and chemoselective ruthenium(II)-catalyzed hydroarylations ...
Exploring multistep cascade reactions triggered by C–H activation are recognized as appealing, yet c...
The ruthenium-catalyzed coupling reactions of benzamides with alkynes in the presence of acetic acid...
A catalytic meta selective C–H alkylation of arenes is described using a wide range of α-halo carbon...
A highly regioselective alkenylation of indole at the C2-position has been achieved using the Ru(II)...
Ruthenium catalysts enabled C–H bond functionalizations on arenes with challenging secondary alkyl h...
International audienceElectron-rich ruthenium(II) catalysts of type (C5R5)XRuL n are used to perform...
A highly selective and switchable ruthenium-catalyzed <i>ortho</i> C–H alkylation and C–H alkenylati...
Herein we report the regio- and stereoselective synthesis of tetrasubstituted alkenes from N-carbamo...
International audienceThe first use of biologically relevant isoindolinones as weak directing groups...
The ruthenium-catalyzed alkenylation reactions of 2-aminobiphenyls and cumylamine proceed smoothly t...
Alkenes and alcohols are among the most abundant and commonly used organic feedstock in industrial p...
International audienceThe first example of a ruthenium-catalyzed C–H bond alkylation via six-membere...
Cationic ruthenium(II) complexes enabled catalytic twofold C–H bond functionalizations with weakly c...
Organic syntheses based on the activation of C–H bonds catalysed by transition metals (TM) are of gr...
Carboxylate assistance enabled efficient and chemoselective ruthenium(II)-catalyzed hydroarylations ...
Exploring multistep cascade reactions triggered by C–H activation are recognized as appealing, yet c...
The ruthenium-catalyzed coupling reactions of benzamides with alkynes in the presence of acetic acid...
A catalytic meta selective C–H alkylation of arenes is described using a wide range of α-halo carbon...
A highly regioselective alkenylation of indole at the C2-position has been achieved using the Ru(II)...
Ruthenium catalysts enabled C–H bond functionalizations on arenes with challenging secondary alkyl h...
International audienceElectron-rich ruthenium(II) catalysts of type (C5R5)XRuL n are used to perform...
A highly selective and switchable ruthenium-catalyzed <i>ortho</i> C–H alkylation and C–H alkenylati...
Herein we report the regio- and stereoselective synthesis of tetrasubstituted alkenes from N-carbamo...