Substructure Search

589722

CC(n1cnn(-c2ccc(OCC(F)(F)C(F)(F)F)cc2)c1=O)C1(c2ccc(F)cc2F)CO1
Reaction #177393
DOI: 10.1039/C8SC04228D
CC(O)C1(c2ccc(F)cc2F)CO1
Reaction #200903
DOI: 10.1039/C8SC04228D
CC(n1ncn(-c2ccc(OC(F)(F)F)cc2)c1=O)C1(c2ccc(F)cc2F)CO1
Reaction #204590
DOI: 10.1039/C8SC04228D
CC(n1ncn(-c2ccc(N3CCN(Cc4ccccc4)CC3)cc2)c1=O)C1(c2ccc(F)cc2F)CO1
Reaction #212677
DOI: 10.1039/C8SC04228D
CC(Oc1ncnn1-c1ccc(OC(F)(F)F)cc1)C1(c2ccc(F)cc2F)CO1
Reaction #213423
DOI: 10.1039/C8SC04228D
C[C@@H](O)C1(c2ccc(F)cc2F)CO1
Reaction #216294
(1R)-1-[2-(2,4-difluorophenyl)-2-oxiranyl]ethanol
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](OC(=O)c1cc([N+](=O)[O-])cc([N+](=O)[O-])c1)[C@@]1(c2ccc(F)cc2F)CO1
Reaction #216295
[(1R)-1-[(2R)-2-(2,4-difluorophenyl)- 2-oxiranyl]ethyl]3,5-dinitrobenzoate
Yield 46.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](OC(=O)c1ccccc1)[C@@]1(c2ccc(F)cc2F)CO1
Reaction #216296
[(1S)-1-[(2R)-2-(2,4-difluorophenyl)-2-oxiranyl]ethyl]benzoate
Yield 78.5%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](O)[C@@]1(c2ccc(F)cc2F)CO1
Reaction #216297
(1S)-1-[(2R)-2-(2,4-difluorophenyl)- 2-oxiranyl]ethanol
Yield 92.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](n1ccn(C)c1=O)[C@@]1(c2ccc(F)cc2F)CO1
Reaction #216298
1-[(1R,2S)-2-(2,4-difluorophenyl)-2,3-epoxy-1-methylpropyl]-3-methyl-2(1H,3H)-imidazolone
Yield 17.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](Oc1nccn1-c1ccc(F)cc1)[C@@]1(c2ccc(F)cc2F)CO1
Reaction #216299
(2R)-2-(2,4-difluorophenyl)-2-[(1R)-1-[1-(4-fluorophenyl)-2-imidazolyloxy]ethyl]oxirane
Yield 31.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](Oc1nccn1-c1ccc(F)cc1F)[C@@]1(c2ccc(F)cc2F)CO1
Reaction #216300
(2R)-2-(2,4-difluorophenyl)- 2-[(1R)-1-[1-(2,4-difluorophenyl)-2-imidazolyloxy]ethyl]oxirane
Yield 27.4%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](n1ncn(-c2ccc(F)cc2)c1=O)[C@@]1(c2ccc(F)cc2F)CO1
Reaction #216301
2-[(1R,2S)-2-(2,4-difluorophenyl)-2,3-epoxy-1-methylpropyl]-4-(4-fluorophenyl)-3(2H,4H)-1,2,4-triazolone
Yield 30.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-n2ccn([C@H](C)[C@@]3(c4ccc(F)cc4F)CO3)c2=O)cc1
Reaction #216302
1-[(1R,2S)-2-(2,4-difluorophenyl)-2,3-epoxy-1-methylpropyl]-3-(4-methoxyphenyl)-2(1H,3H)-imidazolone
Yield 25.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](Oc1nccn1-c1ccc(OC(F)(F)F)cc1)[C@@]1(c2ccc(F)cc2F)CO1
Reaction #216303
(2R)-2-(2,4-difluorophenyl)-2-[(1R)-1-[1-(4-trifluoromethoxyphenyl)-2-imidazolyloxy]ethyl]oxirane
Yield 20.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](n1ncn(-c2ccc(C(F)(F)F)cc2)c1=O)[C@@]1(c2ccc(F)cc2F)CO1
Reaction #216304
2-[(1R,2S)-2-(2,4-difluorophenyl)-2,3-epoxy-1-methylpropyl]-4-(4-trifluoromethylphenyl)-3(2H,4H)-1,2,4-triazolone
Yield 37.5%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](Oc1ncnn1-c1ccc(C(F)(F)F)cc1)[C@@]1(c2ccc(F)cc2F)CO1
Reaction #216305
(2R)-2-(2,4-difluorophenyl)-2-[(1R}-1-[1-(4-trifluoromethylphenyl)-1H-1,2,4-triazol-5-yloxy]ethyl]oxirane
Yield 13.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](n1ncn(-c2ccc(OC(F)(F)F)cc2)c1=O)[C@@]1(c2ccc(F)cc2F)CO1
Reaction #216306
2-[(1R,2S)-2-(2,4-difluorophenyl)-2,3-epoxy-1-methylpropyl]-4-(4-trifluoromethoxyphenyl)-3(2H,4H)-1,2,4-triazolone
Yield 62.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1ccc(-n2ccnc2O[C@H](C)[C@@]2(c3ccc(F)cc3F)CO2)cc1
Reaction #216307
(2R)-2-(2,4-difluorophenyl)-2-[(1R)-1-[1-(4-isopropylphenyl)-2-imidazolyloxy]ethyl] oxiran
Yield 13.9%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](n1ncn(-c2ccc(F)cc2F)c1=O)[C@@]1(c2ccc(F)cc2F)CO1
Reaction #216308
2-[(1R,2S)-2-(2,4-difluorophenyl)-2,3-epoxy-1-methylpropyl]-4-(2,4-difluorophenyl)-3(2H, 4H)-1,2,4-triazolone
Yield 58.3%DOI: 10.6084/m9.figshare.5104873.v1
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