Teilstruktursuche

357910

CC(C)(C)C(=O)OCC(F)(F)S(=O)(=O)[O-].c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #511511
triphenylsulfonium 2-(pivaloyloxy)-1,1-difluoroethanesulfonate
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)OCC(F)(F)S(=O)(=O)[O-].CC(C)(C)c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #511512
4-tert-butylphenyldiphenylsulfonium 2-(pivaloyloxy)-1,1-difluoroethanesulfonate
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)([O-])C(F)(F)CO.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #511513
triphenylsulfonium 1,1-difluoro-2-hydroxy-ethanesulfonate
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)([O-])C(F)(F)CO.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #511514
triphenylsulfonium 1,1-difluoro-2-hydroxy-ethanesulfonate
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OC12CC3CC(C1)CC(C(=O)OCC(F)(F)S(=O)(=O)[O-])(C3)C2.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #511515
triphenylsulfonium 1,1-difluoro-2-(3-methacryloyloxy-adamantane-1-carbonyloxy)-ethane-1-sulfonate
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #643429
oil
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)OCC(F)(F)S(=O)(=O)[O-].c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #645227
compound
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)([O-])C(F)(F)CO.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #645228
triphenylsulfonium 1,1-difluoro-2-hydroxy-ethanesulfonate
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc([S+](c2ccccc2)c2ccccc2)cc1.O=S(=O)([O-])C(F)(F)C(O)C(F)(F)F
Reaction #676725
4-fluorophenyldiphenylsulfonium 1,1,3,3,3-pentafluoro-2-hydroxypropane-1-sulfonate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)OCC(F)(F)S(=O)(=O)[O-].c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #995259
compound
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCC(F)(F)S(=O)(=O)[O-])C12CC3CC(CC(C3)C1)C2.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #995260
compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)OCC(F)(F)S(=O)(=O)[O-].CC(C)(C)c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #995261
compound
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc([S+](c2ccccc2)c2ccccc2)cc1.O=C(OCC(F)(F)S(=O)(=O)[O-])C12CC3CC(CC(C3)C1)C2
Reaction #995262
compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)([O-])C(F)(F)CO.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #995263
triphenylsulfonium 1,1-difluoro-2-hydroxyethanesulfonate
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2CC3CC1CC(C(=O)OCC(F)(F)S(=O)(=O)[O-])(C3)C2.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #995264
triphenylsulfonium 2-(4-adamantanone-1-carbonyloxy)-1,1-difluoroethanesulfonate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)OCC(F)(F)S(=O)(=O)[O-].c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #997151
compound
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCC(F)(F)S(=O)(=O)[O-])C12CC3CC(CC(C3)C1)C2.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #997152
compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)OCC(F)(F)S(=O)(=O)[O-].CC(C)(C)c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #997153
compound
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc([S+](c2ccccc2)c2ccccc2)cc1.O=C(OCC(F)(F)S(=O)(=O)[O-])C12CC3CC(CC(C3)C1)C2
Reaction #997154
compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)([O-])C(F)(F)CO.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #997155
triphenylsulfonium 1,1-difluoro-2-hydroxy-ethanesulfonate
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter