International audienceHere we describe a ruthenium-catalyzed regioselective hydrohaloge-nation reaction of alkynes under mild conditions. Commercially simple halogen sources such as KI, ZnBr2, and ZnCl2 were employed to achieve this transformation. Alkynes derived from bioactive molecules such as L-(-)-borneol, L-menthol, and estrone were also suitable for the transformation, demonstrating the potential synthetic value of this new reaction in organic synthesis
In contrast to all other transition-metal-catalyzed hydrostannation reactions documented in the lite...
The hydrotelluration reaction of alkynes is reviewed. The transformation of vinylic tellurides into ...
Identifying the important roles that functional groups play when substituted alkynes are placed unde...
The ruthenium-catalyzed hydroarylation of alkynes with benzamides proceeds regio- and stereoselectiv...
International audienceAn efficient, novel and direct access to 1-halo-1,3-butadienes is developed. T...
Un des défis majeurs du 21ème siècle sera l'économie d'énergie, c'est pourquoi nous recherchons actu...
By using tandem Ru-catalysis, internal alkynes can be coupled with aldehydes for the synthesis of β,...
Benzylthioethers react with internal alkynes in the presence of catalytic amounts of [Ru(cymene)Cl2]...
The classical repertoire of synthetic organic chemistry is short of methods that allow triple bonds ...
The classical repertoire of synthetic organic chemistry is short of methods that allow triple bonds ...
Benzylthioethers react with internal alkynes in the presence of catalytic amounts of [Ru(cymene)Cl...
Described herein are two different methods for the synthesis of vinyl halides by a shuttle catalysis...
The optimization and substrate scope of ClRh(PPh₃)₃-catalyzed alkyne hydrothiolation with alkane thi...
[Cp*RuCl]4 catalyzes the addition of iPr3SiC≡CX (X = H, Cl) across internal alkynes with formation o...
The optimization and substrate scope of ClRh(PPh₃)₃-catalyzed alkyne hydrothiolation with alkane thi...
In contrast to all other transition-metal-catalyzed hydrostannation reactions documented in the lite...
The hydrotelluration reaction of alkynes is reviewed. The transformation of vinylic tellurides into ...
Identifying the important roles that functional groups play when substituted alkynes are placed unde...
The ruthenium-catalyzed hydroarylation of alkynes with benzamides proceeds regio- and stereoselectiv...
International audienceAn efficient, novel and direct access to 1-halo-1,3-butadienes is developed. T...
Un des défis majeurs du 21ème siècle sera l'économie d'énergie, c'est pourquoi nous recherchons actu...
By using tandem Ru-catalysis, internal alkynes can be coupled with aldehydes for the synthesis of β,...
Benzylthioethers react with internal alkynes in the presence of catalytic amounts of [Ru(cymene)Cl2]...
The classical repertoire of synthetic organic chemistry is short of methods that allow triple bonds ...
The classical repertoire of synthetic organic chemistry is short of methods that allow triple bonds ...
Benzylthioethers react with internal alkynes in the presence of catalytic amounts of [Ru(cymene)Cl...
Described herein are two different methods for the synthesis of vinyl halides by a shuttle catalysis...
The optimization and substrate scope of ClRh(PPh₃)₃-catalyzed alkyne hydrothiolation with alkane thi...
[Cp*RuCl]4 catalyzes the addition of iPr3SiC≡CX (X = H, Cl) across internal alkynes with formation o...
The optimization and substrate scope of ClRh(PPh₃)₃-catalyzed alkyne hydrothiolation with alkane thi...
In contrast to all other transition-metal-catalyzed hydrostannation reactions documented in the lite...
The hydrotelluration reaction of alkynes is reviewed. The transformation of vinylic tellurides into ...
Identifying the important roles that functional groups play when substituted alkynes are placed unde...