#798482

CCOC(=O)c1nc(C)sc1I
Reaction #173845
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(C2CNC(=O)C2)cc1I
Reaction #197774
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc2c(C#N)cccc2c1I
Reaction #233169
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCC1CCC(CCC2CCC(c3ccc(I)cc3)CC2)CC1
Reaction #276841
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1cc(N(C)S(C)(=O)=O)ccc1I
Reaction #343791
N-(4-iodo-3-methylphenyl)-N-methylmethanesulphonamide
Ausbeute 340.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_11
Brc1ccc(-c2ccc(I)cc2)cc1
Reaction #423255
solid
Ausbeute 325.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CCC[C@H]1CC[C@H](CC[C@H]2CC[C@H](c3ccc(I)cc3)CC2)CC1
Reaction #429529
4-(trans-4-(2-(trans-4-n-propylcyclohexyl)ethyl)cyclohexyl)iodobenzene
Ausbeute 21.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
CCCc1ccc([C@H]2CC[C@H](CCc3ccc(I)cc3)CC2)cc1
Reaction #429534
4-(2-(trans-4-(4-n-propylphenyl)cyclohexyl)ethyl)iodobenzene
Ausbeute 118.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
CCCc1ccc(CC[C@H]2CC[C@H](CCc3ccc(I)cc3)CC2)cc1
Reaction #429537
4-(2-(trans-4-(2-(4-n-propylphenyl)ethyl)cyclohexyl)ethyl)iodobenzene
Ausbeute 46.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
Nc1nc(=O)n([C@@H]2CO[C@H](CO)[C@H]2CO)cc1I
Reaction #460917
title compound
Ausbeute 73.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_11
Brc1ccc(-c2ccc(I)cc2)cc1
Reaction #648956
solid
Ausbeute 325.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
Cc1ccccc1C(CCCI)c1ccccc1C
Reaction #653644
title compound 34a
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_01
Cc1ccccc1C(=CCCI)c1ccccc1C
Reaction #653645
title compound 36a
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_01
CC(=O)Nc1[nH]ncc1I
Reaction #675740
title compound
Ausbeute 348.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CC(=O)Nc1[nH]nc(C)c1I
Reaction #675755
title compound
Ausbeute 231.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CC(=O)Nc1[nH]nc(C(F)(F)F)c1I
Reaction #675766
title compound
Ausbeute 296.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CC(=O)Nc1c(I)c(-c2ccccc2)nn1C(C)=O
Reaction #675777
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CC(=O)Nc1[nH]nc(-c2cccc(F)c2)c1I
Reaction #675796
title compound
Ausbeute 368.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CCOC(=O)Cn1nc(-c2ccccc2)c(I)c1NC(C)=O
Reaction #675802
title compound
Ausbeute 352.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
Cc1ccccc1C(CCCI)c1ccccc1C
Reaction #697802
title compound 34a
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_12
Seite 1Weiter