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2697

CC(=O)c1sc(N)nc1C(F)(F)F
Reaction #2897
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(-c2ccc([N+](=O)[O-])c(F)c2)no1
Reaction #162976
title compound
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCOc1ccc([I+]c2ccccc2)cc1.Cc1ccc(S(=O)(=O)[O-])cc1
Reaction #216835
(4-octyloxyphenyl)phenyliodonium tosylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)C(OS(=O)(=O)c1ccc(C)cc1)c1c([N+](=O)[O-])cc(C(F)(F)F)cc1[N+](=O)[O-]
Reaction #442487
pure product
Ausbeute 25.3%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)c1ccc(-c2cnn(Cc3ccccc3)c(=O)c2-c2ccc(F)cc2)cc1
Reaction #469054
sulfoxide
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #481954
solid
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(N)nc1-c1ccccc1
Reaction #481960
title compound
Ausbeute 75.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(N)nc1-c1ccccc1
Reaction #697302
title compound
Ausbeute 75.9%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCOc1ccc([I+]c2ccccc2)cc1.Cc1ccccc1S(=O)(=O)[O-]
Reaction #700770
(4-octyloxyphenyl)phenyl iodonium toluenesulfonate
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cc2c(cc1C)CC(=O)CCC2
Reaction #805995
N-(3-methyl-6-oxo-6,7,8,9-tetrahydro-5H-benzo[7]annulen-2-yl)acetamide
Ausbeute 68.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)O)cc1
Reaction #949333
p-toluenesulfonic acid
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)c1ccc(-c2cnn(Cc3ccccc3)c(=O)c2-c2ccc(F)cc2)cc1
Reaction #978466
sulfoxide
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1sc(N)nc1C(F)(F)F
Reaction #1062225
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(N)nc1-c1cccc([N+](=O)[O-])c1
Reaction #1149858
title compound
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCOc1ccc([I+]c2ccccc2)cc1.Cc1ccc(S(=O)(=O)[O-])cc1
Reaction #1166228
(4-octyloxyphenyl)-phenyliodonium tosylate
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)c1ccc(-c2cnn(Cc3ccccc3)c(=O)c2-c2ccc(F)cc2)cc1
Reaction #1328919
sulfoxide
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)C(OS(=O)(=O)c1ccc(C)cc1)c1c([N+](=O)[O-])cc(C(F)(F)F)cc1[N+](=O)[O-]
Reaction #1361978
pure product
Ausbeute 25.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CO)c1ccccc1I
Reaction #1438872
2-hydroxy-1-(2-iodophenyl)ethanone
Ausbeute 12.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)OCC(=O)c2cc3ccc4cc(Br)ccc4c3s2)cc1
Reaction #1608986
desired compound ( 11d )
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)O)cc1
Reaction #1824083
p-toluenesulfonic acid
DOI: 10.6084/m9.figshare.5104873.v1
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