I agree Our site saves small pieces of text information (cookies) on your device in order to deliver better content and for statistical purposes. You can disable the usage of cookies by changing the settings of your browser. By browsing our website without changing the browser settings you grant us permission to store that information on your device.
Triphenylphosphine sulfide involves in the , conversion of epoxides to episulfides (thiiranes) in presence of TFA of the same stereochemistry. It acts as a ligand for the Pd-catalyzed bisalkoxycarbonylation of olefins.
W. W. Schweikert; Edward A. Meyers. Crystal structure of the triphenylphosphine sulfide-iodine addition complex. J. Phys. Chem.1968, 72 (5), 1561-1565.
B. Ziemer; A. Rabis and H.-U. Steinberger. Triclinic polymorphs of triphenylphosphine and triphenylphosphine sulfide. Acta Cryst.2000, C56 e58-e59.
In the presence of TFA, converts epoxides to episulfides (thiiranes) of the same stereochemistry: J. Am. Chem. Soc., 94, 2880 (1972).
The Pd-catalyzed bisalkoxycarbonylation of olefins gives improved yields in the presence of triphenylphosphine sulfide as a ligand. The phosphine oxide and selenide were significantly less effective, and no product was obtained with triphenylphosphine itself: Tetrahedron Lett, 39, 7529 (1998):
Hazard Statements: H302-H312
Harmful if swallowed. Harmful in contact with skin.
Precautionary Statements: P264b-P270-P280-P301+P312-P302+P352-P312-P330-P363-P501c
Wash face, hands and any exposed skin thoroughly after handling Do not eat, drink or smoke when using this product. Wear protective gloves/protective clothing/eye protection/face protection. IF SWALLOWED: Call a POISON CENTER or doctor/physician if you feel unwell. IF ON SKIN: Wash with plenty of soap and water. Rinse mouth. Wash contaminated clothing before reuse. Dispose of contents/ container to an approved waste disposal plant