Substructure Search

22936

FC(F)(F)c1ccc(-c2cccc(SC3CCCC3)c2)cc1
Reaction #53562
[3-(4-trifluoromethylphenyl)phenyl] cyclopentyl sulfide
Yield 78.0%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1ccc(-c2cccc(SC3CCCC3)c2)cc1
Reaction #204895
DOI: 10.1039/C8SC04228D
FC(F)(F)c1ccc(-c2cccc(SC3CCCC3)c2)cc1
Reaction #586129
[3-(4-trifluoromethylphenyl)phenyl] cyclopentyl sulfide
Yield 78.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CC1(NC(=O)C2CC(S(=O)(=O)c3cccc(-c4ccnc(Cl)c4)c3)CC2C(=O)N2CCC(F)(F)C2)CC1
Reaction #915197
DOI: 10.1039/C8SC04228D
Cc1cccc(S(=O)(=O)C2CC(C(=O)NC3(C#N)CC3)C(C(=O)N3CCC(F)(F)C3)C2)c1
Reaction #1217098
DOI: 10.1039/C8SC04228D
CCOC(=O)[C@@H]1C[C@@H](Sc2cccc(Br)c2)C[C@H]1C(=O)N1CCC(F)(F)C1
Reaction #1454755
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#CC1(NC(=O)[C@@H]2C[C@@H](S(=O)(=O)c3cccc(Br)c3)C[C@H]2C(=O)N2CCC(F)(F)C2)CC1
Reaction #1454756
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2cccc(S(=O)(=O)[C@@H]3C[C@@H](C(=O)NC4(C#N)CC4)[C@H](C(=O)N4CCC(F)(F)C4)C3)c2)ccn1
Reaction #1454764
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#CC1(NC(=O)[C@@H]2C[C@@H](S(=O)(=O)c3cccc(-c4ccnc(Cl)c4)c3)C[C@H]2C(=O)N2CCC(F)(F)C2)CC1
Reaction #1454765
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(S(=O)(=O)[C@@H]2C[C@@H](C(=O)NC3(C#N)CC3)[C@H](C(=O)N3CCC(F)(F)C3)C2)c1
Reaction #1454766
title compound
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1ccc(-c2cccc(SC3CCCC3)c2)cc1
Reaction #1519924
[3-(4-trifluoromethylphenyl)phenyl] cyclopentyl sulfide
Yield 78.0%DOI: 10.6084/m9.figshare.5104873.v1
Brc1cccc(SC2CCCC2)c1
Reaction #1635230
DOI: 10.1039/C8SC04228D
FC(F)(F)c1ccc(-c2cccc(SC3CCCC3)c2)cc1
Reaction #1722904
[3-(4-trifluoromethylphenyl)phenyl]cyclopentyl sulfide
Yield 78.0%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1ccc(-c2cccc(SC3CCCC3)c2)cc1
Reaction #1910338
[3-(4-trifluoromethylphenyl)phenyl]cyclopentyl sulfide
Yield 78.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(Br)cc(SC2CCCC2)c1
Reaction #1932425
crude product
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Br)cc(SC2CCCC2)c1
Reaction #1932426
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(-c2ccc(C)cc2)cc(S(=O)(=O)C2CCCC2)c1
Reaction #1932427
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Brc1cccc(SC2CCCC2)c1
Reaction #2205519
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Ic1cccc(SC2CCCC2)c1
Reaction #2205520
title compound
Yield 42.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(Sc2cccc(Br)c2)CC1C(=O)N1CCC(F)(F)C1
Reaction #2431998
DOI: 10.1039/C8SC04228D