Transition Metal Catalysts

Me₃(OMe)tBuXPhos.

Mercuric ammonium chloride.

Mercuric ammonium chloride.

Mercuric ammonium chloride.

Mercuric ammonium chloride.

Polyene cyclization, oxymercuration, catalytic hydration of alkynes, catalytic hydrative enyne cyclization, catalytic arylyne cyclization, catalytic biomimetic tandem cyclization, catalyticketoalkyne cyclization leading to furans, catalytic

Polyene cyclization, oxymercuration, catalytic hydration of alkynes, catalytic hydrative enyne cyclization, catalytic arylyne cyclization, catalytic biomimetic tandem cyclization, catalyticketoalkyne cyclization leading to furans, catalytic

Polyene cyclization, oxymercuration, catalytic hydration of alkynes, catalytic hydrative enyne cyclization, catalytic arylyne cyclization, catalytic biomimetic tandem cyclization, catalyticketoalkyne cyclization leading to furans, catalytic

Polyene cyclization, oxymercuration, catalytic hydration of alkynes, catalytic hydrative enyne cyclization, catalytic arylyne cyclization, catalytic biomimetic tandem cyclization, catalyticketoalkyne cyclization leading to furans, catalytic

DescriptionCatalyst for addition of HSCN to alkynes.Mercury(II) thiocyanate has been used for the determination of the chloride ions by colorimetric method.It can be employed as a reactant for the synthesis of:Polymeric mercury(II) coordination

DescriptionCatalyst for addition of HSCN to alkynes.Mercury(II) thiocyanate has been used for the determination of the chloride ions by colorimetric method.It can be employed as a reactant for the synthesis of:Polymeric mercury(II) coordination

DescriptionCatalyst for addition of HSCN to alkynes.Mercury(II) thiocyanate has been used for the determination of the chloride ions by colorimetric method.It can be employed as a reactant for the synthesis of:Polymeric mercury(II) coordination