Improsulfan tosilate

p -Toluenesulfonyl azide is used as a nitrene source and in the synthesis of N -sulfimines, N -tosylphosphinimines, and N -sulfoximines. Application p -Toluenesulfonyl azide solution can be employed as a reagent along with alkyne, and amine in the

CH₃C₆H₄SO₂Cl CAS#: 98-59-9 F.W.: 190.65 Tosyl chloride

CH₃C₆H₄SO₂Cl CAS#: 98-59-9 F.W.: 190.65 Tosyl chloride

p -Toluenesulfonyl isocyanate undergoes palladium-catalyzed bis-allylation reaction with allylstannanes and allyl chlorides . Application p -Toluenesulfonyl isocyanate has been used as : derivatization reagent in determination of 3-&#945-hydroxy

p -Toluenesulfonyl isocyanate undergoes palladium-catalyzed bis-allylation reaction with allylstannanes and allyl chlorides . Application p -Toluenesulfonyl isocyanate has been used as : derivatization reagent in determination of 3-&#945-hydroxy

p -Toluenesulfonyl isocyanate undergoes palladium-catalyzed bis-allylation reaction with allylstannanes and allyl chlorides . Application p -Toluenesulfonyl isocyanate has been used as : derivatization reagent in determination of 3-&#945-hydroxy

Sodium p-toluenesulfinate

Sodium p-toluenesulfinate

Sodium p-toluenesulfinate

Sodium p-toluenesulfinate

Application tert -Butyldimethylsilanol can be used as a silylating agent for the protection of hydroxyl groups via silylation. It is used: For the preparation of &#945- chiral ether derivatives by catalytic asymmetric allylic substitution.

Application tert -Butyldimethylsilanol can be used as a silylating agent for the protection of hydroxyl groups via silylation. It is used: For the preparation of &#945- chiral ether derivatives by catalytic asymmetric allylic substitution.