Recherche de Sous-structure

2700

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Reaction #3010
glass
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)[O-])cc1.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #3012
salt
Rendement 73.1%DOI: 10.6084/m9.figshare.5104873.v1
C=COCCOc1ccc([S+](c2ccc(C(C)(C)C)cc2)c2ccc(C(C)(C)C)cc2)cc1.CC(C)c1cc(C(C)C)c(S(=O)(=O)[O-])c(C(C)C)c1
Reaction #834829
4-vinyloxyethoxyphenyldi(4-t-butylphenyl)sulfonium 2,4,6-triisopropylbenzenesulfonate salt
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)[O-])cc1.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #1255190
triphenylsulfonium p-toluenesulfonate
Rendement 85.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)[O-])cc1.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #1255194
triphenylsulfonium p-toluenesulfonate
Rendement 113.2%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)([O-])c1ccc(C(F)(F)F)cc1.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #1255200
target compound
Rendement 76.8%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1ccc([S+](c2ccc(OC(C)(C)C)cc2)c2ccc(OC(C)(C)C)cc2)cc1.Cc1ccc(S(=O)(=O)[O-])cc1
Reaction #1544604
bis(4-tert-butoxyphenyl)(4-dimethylaminophenyl)sul fonium p-toluenesulfonate
Rendement 49.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)[O-])cc1.Oc1ccc([S+](c2ccccc2)c2ccc(O)cc2)cc1
Reaction #1576669
bis(p-hydroxyphenyl)phenylsulfonium p-toluenesulfonate
Rendement 100.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)[O-])cc1.Oc1ccc([S+](c2ccc(O)cc2)c2ccc(O)cc2)cc1
Reaction #1576670
tris(p-hydroxyphenyl)sulfonium p-toluenesulfonate
Rendement 97.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)[O-])cc1.Oc1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #1840853
target compound
Rendement 108.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)[O-])cc1.Fc1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #2007797
4-fluorophenyldiphenylsulfonium 4-toluene-sulfonate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)[O-])cc1.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #2144314
triphenylsulfonium p-toluenesulfonate
Rendement 85.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)[O-])cc1.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #2144318
triphenylsulfonium p-toluenesulfonate
Rendement 113.2%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)([O-])c1ccc(C(F)(F)F)cc1.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #2144324
target compound
Rendement 76.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)[O-])cc1.Cc1ccccc1[S+](c1ccccc1)c1ccccc1
Reaction #2173086
diphenyl-o-methylphenylsulfonium p-toluenesulfonate
Rendement 91.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)([O-])c1ccc(Cc2ccccc2)cc1.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #2315549
triphenylsulfonium 4-phenylmethylbenzenesulfonate
Rendement 52.0%DOI: 10.6084/m9.figshare.5104873.v1
C=COCCOc1ccc([S+](c2ccc(C(C)(C)C)cc2)c2ccc(C(C)(C)C)cc2)cc1.CC(C)c1cc(C(C)C)c(S(=O)(=O)[O-])c(C(C)C)c1
Reaction #2352969
4-vinyloxyethoxyphenyldi(4-t-butylphenyl)sulfonium 2,4,6-triisopropylbenzenesulfonate
DOI: 10.6084/m9.figshare.5104873.v1
C=COCCOc1ccc([S+](c2ccccc2)c2ccccc2)cc1.CC(C)c1cc(C(C)C)c(S(=O)(=O)[O-])c(C(C)C)c1
Reaction #2352970
4-vinyloxyethoxyphenyldiphenylsulfonium 2,4,6-triisopropylbenzenesulfonate
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C(=O)OC(C(F)(F)F)C(F)(F)S(=O)(=O)[O-].Oc1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #2448718
4-hydroxyphenyldiphenylsulfonium 1,1,3,3,3-pentafluoro-2-(methacryloyloxy)propane-1-sulfonate
DOI: 10.6084/m9.figshare.5104873.v1