International audienceAn unprecented N- and C(3)-dialkylation of unactivated amines by a cascade reaction via borrowing hydrogen methodology using new (arene)ruthenium(II) complexes featuring phosphinosulfonate ligands is described. This reaction is highly regioselective and produces water as the only side product
A simple and environmentally benign procedure for the synthesis of secondary amines in water has bee...
International audienceStraighforward access to various saturated amines from allylic alcohols and is...
International audienceStraighforward access to various saturated amines from allylic alcohols and is...
International audienceAn unprecented N- and C(3)-dialkylation of unactivated amines by a cascade rea...
International audienceAn unprecented N- and C(3)-dialkylation of unactivated amines by a cascade rea...
International audienceA selective C(3)-alkylation via activation/functionalization of sp(3) C-H bond...
International audienceA selective C(3)-alkylation via activation/functionalization of sp(3) C-H bond...
International audienceA selective C(3)-alkylation via activation/functionalization of sp(3) C-H bond...
The alkylation of amines by alcohols has been achieved using 0.5 mol % [Ru(p-cymene)Cl(2)](2) with t...
A new ruthenium complex catalyzes the amination of primary and secondary alcohols and the regioselec...
A new ruthenium complex catalyzes the amination of primary and secondary alcohols and the regioselec...
International audienceStraighforward access to various saturated amines from allylic alcohols and is...
A simple and environmentally benign procedure for the synthesis of secondary amines in water has bee...
A simple and environmentally benign procedure for the synthesis of secondary amines in water has bee...
A new ruthenium complex catalyzes the amination of primary and secondary alcohols and the regioselec...
A simple and environmentally benign procedure for the synthesis of secondary amines in water has bee...
International audienceStraighforward access to various saturated amines from allylic alcohols and is...
International audienceStraighforward access to various saturated amines from allylic alcohols and is...
International audienceAn unprecented N- and C(3)-dialkylation of unactivated amines by a cascade rea...
International audienceAn unprecented N- and C(3)-dialkylation of unactivated amines by a cascade rea...
International audienceA selective C(3)-alkylation via activation/functionalization of sp(3) C-H bond...
International audienceA selective C(3)-alkylation via activation/functionalization of sp(3) C-H bond...
International audienceA selective C(3)-alkylation via activation/functionalization of sp(3) C-H bond...
The alkylation of amines by alcohols has been achieved using 0.5 mol % [Ru(p-cymene)Cl(2)](2) with t...
A new ruthenium complex catalyzes the amination of primary and secondary alcohols and the regioselec...
A new ruthenium complex catalyzes the amination of primary and secondary alcohols and the regioselec...
International audienceStraighforward access to various saturated amines from allylic alcohols and is...
A simple and environmentally benign procedure for the synthesis of secondary amines in water has bee...
A simple and environmentally benign procedure for the synthesis of secondary amines in water has bee...
A new ruthenium complex catalyzes the amination of primary and secondary alcohols and the regioselec...
A simple and environmentally benign procedure for the synthesis of secondary amines in water has bee...
International audienceStraighforward access to various saturated amines from allylic alcohols and is...
International audienceStraighforward access to various saturated amines from allylic alcohols and is...