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1250822

CC(C)(C)OC(=O)N1CCC2C(C1)c1cc(-c3ccc(C(F)(F)F)cc3Cl)cc3c1N2CCC3
Reaction #229226
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC2C(C1)c1cc(-c3ccc(C(F)(F)F)cc3Cl)cc3c1N2CCC3
Reaction #269424
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC2C(C1)c1cc(-c3ccc(C(F)(F)F)cc3Cl)cc3c1N2CC3
Reaction #377582
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC2C(C1)c1cc(-c3ccc(C(F)(F)F)cc3Cl)cc3c1N2CC3
Reaction #408491
DOI: 10.1039/C8SC04228D
Nc1ccc(-c2ccc(C(F)(F)F)cc2Cl)cc1
Reaction #492431
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C(=O)OCC)c1cccc(-c2ccc(C(F)(F)F)cc2Cl)c1
Reaction #715655
title compound
Ausbeute 64.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Cc1cccc(-c2ccc(C(F)(F)F)cc2Cl)c1
Reaction #715656
title compound
Ausbeute 49.6%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1c(-c2ccc(C(F)(F)F)cc2Cl)ccnc1OCc1ccccc1
Reaction #921632
DOI: 10.1039/C8SC04228D
CC(C)(C)c1cc(C=O)c(O)c(-c2ccc(C(F)(F)F)cc2Cl)c1
Reaction #1016746
5-(tert-Butyl)-2′-chloro-2-hydroxy-4′-(trifluoromethyl)-[1,1′-biphenyl]-3-carbaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCN(C)c1nc2ccc(NC(=O)c3ccc(-c4ccc(C(F)(F)F)cc4Cl)cc3)cc2s1
Reaction #1262176
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCN(C)c1nc2ccc(NC(=O)c3ccc(-c4ccc(C(F)(F)F)cc4Cl)cc3)cc2s1
Reaction #1302463
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CC[C@@H]2[C@H](C1)c1cc(-c3ccc(C(F)(F)F)cc3Cl)cc3c1N2CC3
Reaction #1353243
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC[C@@H]2[C@H](C1)c1cc(-c3ccc(C(F)(F)F)cc3Cl)cc3c1N2CCC3
Reaction #1353250
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC[C@@H]2[C@H](C1)c1cc(-c3ccc(C(F)(F)F)cc3Cl)cc3c1N2CC3
Reaction #1380055
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC[C@@H]2[C@H](C1)c1cc(-c3ccc(C(F)(F)F)cc3Cl)cc3c1N2CCC3
Reaction #1380062
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(Cl)c(-c2ccc(C(F)(F)F)cc2Cl)cc1[N+](=O)[O-]
Reaction #1555336
5-chloro-4-[2-chloro-4-(trifluoromethyl)phenyl]-2-nitroaniline
Ausbeute 63.8%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1ncns1)c1ccc2c(-c3ccc(C(F)(F)F)cc3Cl)cccc2c1
Reaction #1560477
5-(2-chloro-4-(trifluoromethyl)phenyl)-N-(1,2,4-thiadiazol-5-yl)naphthalene-2-sulfonamide
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1ccncn1)c1ccc2c(-c3ccc(C(F)(F)F)cc3Cl)cccc2c1
Reaction #1560493
5-(2-chloro-4-(trifluoromethyl)phenyl)-N-(pyrimidin-4-yl)naphthalene-2-sulfonamide
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1ncns1)c1ccc2c(-c3ccc(C(F)(F)F)cc3Cl)nccc2c1
Reaction #1560505
1-(2-chloro-4-(trifluoromethyl)phenyl)-N-(1,2,4-thiadiazol-5-yl)isoquinoline-6-sulfonamide
Ausbeute 22.4%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1nccs1)c1ccc2c(-c3ccc(C(F)(F)F)cc3Cl)ncnc2c1
Reaction #1560877
4-(2-chloro-4-(trifluoromethyl)phenyl)-N-(thiazol-2-yl)quinazoline-7-sulfonamide
Ausbeute 23.1%DOI: 10.6084/m9.figshare.5104873.v1
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