#4523839

COC(COc1ccc(F)c(C)c1)OC
Reaction #192786
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cc(Oc2ncc(Cl)cc2C(=O)NC(C)c2ccc(C(=O)OC(C)(C)C)cc2)ccc1F
Reaction #282922
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1cc(Oc2cccc(N(Cc3cccc(OC(F)(F)F)c3)C[C@@H](O)C(F)(F)F)c2)ccc1F
Reaction #480136
(2R)-3-[[3-(4-fluoro-3-methylphenoxy)phenyl][[3-(trifluoromethoxy)phenyl]methyl]amino]-1,1,1-trifluoro-2-propanol
Rendement 23.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_10
Cc1cc(OCC2CCCCN(Cc3ccccc3)C2)ccc1F
Reaction #554653
1-5
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
Cc1cc(OCC2CCCC(C)N(Cc3ccccc3)C2)ccc1F
Reaction #554661
6-[(4-fluoro-3-methylphenoxy)methyl]-1-benzyl-2-methylazepane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
Cc1cc(OCC2COCC(C)N(Cc3ccccc3)C2)ccc1F
Reaction #554670
4-benzyl-6-[(4-fluoro-3-methylphenoxy)methyl]-3-methyl-1,4-oxazepane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
CC(=O)Oc1ccc(F)c(C)c1
Reaction #598090
4-fluoro-3-methylphenyl acetate
Rendement 100.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
Cc1cc(Oc2cccc(N(Cc3cccc(OC(F)(F)F)c3)C[C@@H](O)C(F)(F)F)c2)ccc1F
Reaction #732145
(2R)-3-[[3-(4-fluoro-3-methylphenoxy)phenyl][[3-(trifluoromethoxy)phenyl]methyl]amino]-1,1,1-trifluoro-2-propanol
Rendement 23.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
CCCCC(Oc1ccc(F)c(C)c1)C(=O)OC
Reaction #749359
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCOC(=O)COc1ccc(F)c(C)c1
Reaction #782093
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
Cc1cc(Oc2cccc(N(Cc3cccc(OC(F)(F)F)c3)C[C@@H](O)C(F)(F)F)c2)ccc1F
Reaction #940368
(2R)-3-[[3-(4-fluoro-3-methylphenoxy)phenyl][[3-(trifluoromethoxy)phenyl]methyl]amino]-1,1,1-trifluoro-2-propanol
Rendement 23.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_08
Cc1cc(O[Si](C)(C)C(C)(C)C)ccc1F
Reaction #986422
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_04
Cc1cc(O)c(C#N)cc1F
Reaction #1045291
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
Cc1cc(F)ccc1Oc1ccc(OC(F)(F)F)cc1C(=O)Nc1cc[nH]c(=O)c1
Reaction #1140361
2-(4-fluoro-2-methylphenoxy)-N-(2-oxo-1,2-dihydropyridin-4-yl)-5-(trifluoromethoxy)benzamide
Rendement 43.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_07
Cc1cc(Oc2cccc(N(Cc3cccc(OC(F)(F)F)c3)C[C@@H](O)C(F)(F)F)c2)ccc1F
Reaction #1147246
(2R)-3-[[3-(4-fluoro-3-methylphenoxy)phenyl][[3-(trifluoromethoxy)phenyl] methyl]amino]-1,1,1-trifluoro-2-propanol
Rendement 23.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_02
Cc1cc(Oc2c(Cl)cc([N+](=O)[O-])cc2Cl)ccc1F
Reaction #1201489
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
Cc1cc(O[Si](C)(C)C(C)(C)C)ccc1F
Reaction #1210364
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
Cc1cc(Oc2ccc(C#N)cc2)ccc1F
Reaction #1239060
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
Cc1cc(O[Si](C)(C)C(C)(C)C)ccc1F
Reaction #1266450
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_10
Cc1cc(Oc2cccc(N(Cc3cccc(OC(F)(F)F)c3)C[C@@H](O)C(F)(F)F)c2)ccc1F
Reaction #1331930
(2R)-3-[[3-(4-fluoro-3-methylphenoxy)phenyl][[3-(trifluoromethoxy)phenyl]methyl]amino]-1,1,1-trifluoro-2-propanol
Rendement 23.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_10
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