phenyl trifluoromethanesulfonate
phenyl trifluoromethanesulfonate structure
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Common Name | phenyl trifluoromethanesulfonate | ||
|---|---|---|---|---|
| CAS Number | 17763-67-6 | Molecular Weight | 226.17300 | |
| Density | 1.396 g/mL at 25ºC(lit.) | Boiling Point | 99-100ºC60 mm Hg(lit.) | |
| Molecular Formula | C7H5F3O3S | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | 160 °F | |
| Symbol |
GHS05, GHS06 |
Signal Word | Danger | |
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Enantioselective alpha-arylation of ketones with aryl triflates catalyzed by difluorphos complexes of palladium and nickel.
J. Am. Chem. Soc. 130(1) , 195-200, (2008) The asymmetric alpha-arylation of ketones with aryl triflates is described, and the use of this electrophile with nickel and palladium catalysts containing a segphos derivative increases substantially the scope of highly enantioselective arylations of ketone ... |
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One-pot synthesis of carbazoles by palladium-catalyzed N-arylation and oxidative coupling. Watanabe T, et al.
Chem. Commun. (Camb.) 43 , 4516-4518, (2007)
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Regioselective arylation of benzanilides with aryl triflates or bromides under palladium catalysis. Kametani Y, et al.
Tetrahedron Lett. 41(15) , 2655-2658, (2000)
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Palladium-catalyzed asymmetric arylation of 2, 3-dihydrofuran with phenyl triflate. A novel asymmetric catalysis involving a kinetic resolution process. Ozawa F, et al.
Organometallics 12(10) , 4188-4196, (1993)
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Palladium cross-coupling reactions of aryl fluorosulfonates: an alternative to triflate chemistry. Roth GP and Fuller CE.
J. Org. Chem. 56(11) , 3493-3496, (1991)
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