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1499350

[Br-]
Reaction #263773
DOI: 10.1039/C8SC04228D
CC(C)(C)c1ccc([S+](c2ccc(C(C)(C)C)cc2)c2ccc(C(C)(C)C)cc2)cc1.[Br-]
Reaction #306690
tris(4-tert-butylphenyl)sulfonium bromide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc([S+](c2ccc(C(C)(C)C)cc2)c2ccc(C(C)(C)C)cc2)cc1.[Br-]
Reaction #312584
tris(4-tert-butylphenyl)sulfonium bromide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc([S+](c2ccc(C(C)(C)C)cc2)c2ccc(C(C)(C)C)cc2)cc1.O=S(=O)([O-])C(F)(F)C(F)(F)C(F)(F)C(F)(F)F
Reaction #364872
white crystals
Ausbeute 60.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc([S+](c2ccc(C(C)(C)C)cc2)c2ccc(C(C)(C)C)cc2)cc1.[Br-]
Reaction #511510
tris(4-tert-butylphenyl)sulfonium bromide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc(S(=O)(=O)CCC[CH2][Sn]([CH3])([CH3])[CH3])cc1
Reaction #530541
4-(4-t-butylphenylsulfonyl)butyltrimethylstannane
Ausbeute 20.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc([S+](c2ccc(C(C)(C)C)cc2)c2ccc(C(C)(C)C)cc2)cc1.[Br-]
Reaction #577227
tris(4-tert-butylphenyl)sulfonium bromide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc([S+](c2ccc(C(C)(C)C)cc2)c2ccc(C(C)(C)C)cc2)cc1.[Br-]
Reaction #578427
tris(4-tert-butylphenyl)sulfonium bromide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc([S+](c2ccc(C(C)(C)C)cc2)c2ccc(C(C)(C)C)cc2)cc1.CS(=O)(=O)[O-]
Reaction #631717
tris-(4-t-butylphenyl)sulfonium methane sulfonate
Ausbeute 20.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc([S+](c2ccc(C(C)(C)C)cc2)c2ccc(C(C)(C)C)cc2)cc1.CS(=O)(=O)[O-]
Reaction #631723
tris-(4-t-butylphenyl)sulfonium methane sulfonate
Ausbeute 20.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc([S+](c2ccc(C(C)(C)C)cc2)c2ccc(C(C)(C)C)cc2)cc1.[Br-]
Reaction #640567
tris(4-tert-butylphenyl)sulfonium bromide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc([S+](c2ccc(C(C)(C)C)cc2)c2ccc(C(C)(C)C)cc2)cc1.[Br-]
Reaction #643420
tris(4-tert-butylphenyl)sulfonium bromide
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(C)(C)c2c1ccc(S(=O)c1ccc3c(c1Cc1ccc(C(=O)O)cc1)C(C)(C)CCC3(C)C)c2Cc1ccc(C(=O)O)cc1
Reaction #752651
DOI: 10.1039/C8SC04228D
CC(C)(C)c1ccc(S(=O)(=O)CCC[CH2][Sn]([CH3])([CH3])[CH3])cc1
Reaction #1058880
4-(4-t-butylphenylsulfonyl)butyltrimethylstannane
Ausbeute 20.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc([S+](c2ccc(C(C)(C)C)cc2)c2ccc(C(C)(C)C)cc2)cc1.[Cl-]
Reaction #1354127
tris(4-tert-butylphenyl)sulfonium chloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc(S(=O)(=O)CCC[CH2][Sn]([CH3])([CH3])[CH3])cc1
Reaction #1371043
4-(p-t-butylphenyl-sulfonyl)butyltrimethylstannane
Ausbeute 20.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc([S+](=O)(CC(=O)c2ccccc2)c2ccc(C(C)(C)C)cc2)cc1.CCC(C)[B-](c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #1528107
bis(p-tert-butylphenyl)phenacyloxosulfonium (sec-butyl)triphenylborate
Ausbeute 72.9%DOI: 10.6084/m9.figshare.5104873.v1
C=C[B-](c1ccc(F)cc1)(c1ccc(F)cc1)c1ccc(F)cc1.COC(=O)C(C(=O)OC)=C(C[S+](=O)(c1ccc(C(C)(C)C)cc1)c1ccc(C(C)(C)C)cc1)c1ccccc1
Reaction #1528124
bis(p-tert-butylphenyl)[3,3-bis(methoxycarbonyl)-2-phenyl-2-propenyl]oxosulfonium vinyltris(p-fluorophenyl)borate
Ausbeute 42.4%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC(C)(C)c2c1ccc(S(=O)c1ccc3c(c1Cc1ccc(C(=O)O)cc1)C(C)(C)CCC3(C)C)c2Cc1ccc(C(=O)O)cc1
Reaction #1621480
title compound
Ausbeute 21.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc([S+](c2ccc(C(C)(C)C)cc2)c2ccc(C(C)(C)C)cc2)cc1.[Br-]
Reaction #1727541
tris(4-tert-butylphenyl)sulfonium bromide
DOI: 10.6084/m9.figshare.5104873.v1
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