1,4-Diiodobenzene

Cc1cc(C(c2ccc(O)c(C)c2)C2CC3CC2CC3c2ccc(C3CC4CC3CC4C(c3ccc(O)c(C)c3)c3ccc(O)c(C)c3)cc2)ccc1O
Reaction #68720
4,4′-((5-(4-(5-(bis(4-hydroxy-3-methylphenyl)methyl)bicyclo[2.2.1]heptan-2-yl)phenyl) bicyclo[2.2.1]heptan-2-yl)methylene)bis(2-methylphenol)
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)(C)OC(=O)N1CCCC1c1nc2ccc(C#Cc3ccc(I)cc3)cc2[nH]1
Reaction #158954
2-[6-(4-Iodo-phenylethynyl)-1H-benzoimidazol-2-yl]-pyrrolidine-1-carboxylic acid tert-butyl ester
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)OC(=O)N1CCCC1c1nc2ccc(C#Cc3ccc(I)cc3)cc2[nH]1
Reaction #166908
2-[6-(4-Iodo-phenylethynyl)-1H-benzoimidazol-2-yl]-pyrrolidine-1-carboxylic acid tert-butyl ester
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)C(C)(O)c1ccc(I)cc1
Reaction #177287
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Ic1ccc(OC2CN3CCC2CC3)cc1
Reaction #200393
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Ic1ccc(OC2CN3CCC2CC3)cc1
Reaction #273289
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Ic1ccc(OC2CN3CCC2CC3)cc1
Reaction #302068
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
OC1(c2ccc(I)cc2)CCOCC1
Reaction #317472
tetrahydro-4-(4-iodophenyl)-2H-pyran-4-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
OC1(c2ccc(I)cc2)CCCOCC1
Reaction #317475
4-(4-iodophenyl)oxepan-4-ol
Ausbeute 36.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
O=C(NCCC#Cc1ccc(I)cc1)OCc1ccccc1
Reaction #341546
[4-(4-Iodophenyl)but-3-ynyl]carbamic acid benzyl ester
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
CC(C)(C)OC(=O)N1CCC(Oc2cccc3c2ccn3-c2ccc(I)cc2)CC1
Reaction #394521
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Nc1ccc(C#Cc2ccc(I)cc2)cc1
Reaction #434790
desired product
Ausbeute 354.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
FC(F)=C(F)c1ccc(C(F)=C(F)F)cc1
Reaction #460470
1,4-BIS(TRIFLUOROVINYL)BENZENE
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_11
CC(C)(C)OC(=O)NC(C(=O)c1ccc(I)cc1)c1ccc(Cl)c(Cl)c1
Reaction #472085
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CC(C)(C)OC(=O)NC(C(=O)c1ccc(I)cc1)c1ccc(Cl)c(F)c1
Reaction #472137
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
Cc1cc(C(NC(=O)OC(C)(C)C)C(=O)c2ccc(I)cc2)ccc1Cl
Reaction #472138
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CC(C)(C)OC(=O)NC(C(=O)c1ccc(I)cc1)c1ccc(C(F)(F)F)cc1
Reaction #472139
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
Cc1ccc(C(NC(=O)OC(C)(C)C)C(=O)c2ccc(I)cc2)cc1F
Reaction #472141
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
Cc1ccc(C(NC(=O)OC(C)(C)C)C(=O)c2ccc(I)cc2)cc1Cl
Reaction #472142
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CC(C)(C)OC(=O)NC(C(=O)c1ccc(I)cc1)c1ccc(C(F)(F)F)c(F)c1
Reaction #472143
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
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