Участвует в 457 реакциях

16607

Fc1ccccc1-n1c(COCc2ccccc2)nnc1-c1ccc(-c2ccccc2)cc1
Reaction #7031
3-benzyloxymethyl-5-biphenyl-4-yl-4-(2-fluorophenyl)-4H-1,2,4-triazole
Выход 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COC(=O)c1nn(C)c(=O)cc1Nc1ccccc1F
Reaction #44240
title compound
Выход 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)c1cc([N+](=O)[O-])c(N)c(F)c1Nc1ccccc1F
Reaction #60250
pure desired product
Выход 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
—
Reaction #75285
164
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_11
CC(=Nc1ccccc1F)c1cccc(C(C)=Nc2c(C)cc(C)cc2C)n1
Reaction #78029
2-[1-(2,4,6-trimethylphenylimino)ethyl]-6-[1-(2-fluorophenylimino)ethyl]pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C(O)C1CCN(c2ccccc2F)C1=O
Reaction #86841
yellow solid
Выход 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1nc(NCc2ccccn2)nc(Nc2ccccc2F)c1C
Reaction #91419
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=S(=O)(c1ccccc1)c1cnc2c(F)cccc2c1O
Reaction #159822
4-hydroxy-3-phenylsulfonyl-8-fluoroquinoline
Выход 3.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(=O)Nc1ccccc1F
Reaction #160005
title compound
Выход 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(C=Cc1ccccc1)Nc1ccccc1F
Reaction #162529
N-(2-fluorophenyl)cinnamamide
Выход 103.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
—
Reaction #168368
crude residue
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
N#CSc1ccc(N)c(F)c1
Reaction #180794
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)c1ccc(CNc2ccccc2F)cc1
Reaction #182167
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1nc2c(ncn2C)c(F)c1Nc1ccccc1F
Reaction #184027
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)C(F)(F)F
Reaction #190096
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)c1cnc(Nc2ccccc2F)[nH]c1=O
Reaction #190199
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)C(=NNc1ccccc1F)C(C)=O
Reaction #191756
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)CCNc1ccccc1F
Reaction #199230
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)c1cccnc1Nc1ccccc1F
Reaction #206184
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccnc2c(F)cccc12
Reaction #218812
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
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