triphenylsulfonium chloride

—
Reaction #3009
solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
—
Reaction #3010
glass
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(OC(c1ccccc1)C(F)(F)C(=O)[O-])C12CC3CC(CC(C3)C1)C2.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #86796
triphenylsulfonium 3-(adamantane-1-carbonyloxy)-2,2-difluoro-3-phenyl propionate
Rendimiento 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(OC(C(F)(F)F)C(F)(F)S(=O)(=O)[O-])c1ccccc1.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #312587
triphenylsulfonium 2-benzoyloxy-1,1,3,3,3-pentafluoropropane-1-sulfonate
Rendimiento 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
O=C(OCC12CC3CC(CC(O)(C3)C1)C2)C(F)(F)S(=O)(=O)[O-].c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #420749
triphenylsulfonium 1-((3-hydroxy-1-adamantyl)methoxycarbonyl)difluoromethane sulfonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
—
Reaction #476181
246.9
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
O=S(=O)([O-])C(F)(F)CO.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #492194
triphenylsulfonium 2-hydroxy-1,1-difluoroethanesulfonate
Rendimiento 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
O=C(OC(C(F)(F)F)C(F)(F)S(=O)(=O)[O-])c1ccccc1.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #577230
triphenylsulfonium 2-benzoyloxy-1,1,3,3,3-pentafluoropropane-1-sulfonate
Rendimiento 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
Cc1ccc(S(=O)(=O)OCC(F)(F)S(=O)(=O)[O-])cc1.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #578431
triphenylsulfonium 1,1-difluoro-2-tosyloxyethanesulfonate
Rendimiento 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
O=C([O-])C1(C(F)(F)F)CC2C=CC1C2.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #609528
objective material
Rendimiento 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
O=C1C2CC3CC1CC(OC(=O)C(F)(F)S(=O)(=O)[O-])(C3)C2.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #645229
triphenylsulfonium 4-oxo-1-adamantyloxycarbonyldifluromethanesulfonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
COC(=O)C1CC(C(=O)OC)C(C(F)(F)C(F)(F)S(=O)(=O)[O-])C1.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #712372
triphenylsulfonium 2-(2,4-bis(methoxycarbonyl)cyclopentyl)-1,1,2,2-tetrafluoroethanesulfonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
O=C(OCC(F)(F)S(=O)(=O)[O-])C12CC3CC(CC(C3)C1)C2.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #995260
compound
Rendimiento 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_09
O=C(OCC(F)(F)S(=O)(=O)[O-])C12CC3CC(CC(C3)C1)C2.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #997152
compound
Rendimiento 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_09
—
Reaction #1269192
( 34 )
Rendimiento 43.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_10
C=C(C)C(=O)OC(CC)C(F)(F)C(=O)OCC(F)(F)S(=O)(=O)[O-].c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #1269823
triphenylsulfonium 2-[3-(methacryloyloxy)-2,2-difluoro-n-pentanoyloxy]-1,1-difluoroethanesulfonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_03
COc1cc(S(=O)(=O)[O-])ccc1OS(=O)(=O)c1ccc(C)cc1.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #1354128
triphenylsulfonium 3-methoxy-4-(4′-methylphenyl-sulfonyloxy)benzenesulfonate
Rendimiento 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_04
O=C(OCC12CC3CC(CC(O)(C3)C1)C2)C(F)(F)S(=O)(=O)[O-].c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #1492060
triphenylsulfonium 1-((3-hydroxy-1-adamantyl)methoxycarbonyl)difluoromethane sulfonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
CCOC(=O)C(C#N)C=O.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #1541933
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_01
CC(C)(C)OC(=O)C(C#N)C=O.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #1541934
3-oxo-2-cyanopropanoic acid t-butyl ester triphenylsulfonium salt
Rendimiento 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_01
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