4-fluoroacetophenone

Fc1ccc(-c2cc(-c3ccc(F)cc3)c3ccccc3n2)cc1
Reaction #1245
2,4-bis(4-fluorophenyl)quinoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)c1ccc(Oc2ccc(C(c3ccccc3)(c3ccc(Oc4ccc(C(C)=O)cc4)cc3)C(F)(F)F)cc2)cc1
Reaction #6291
1,1-bis[4-(4-acetylphenoxy)phenyl]-1-phenyl-2,2,2-trifluoroethane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COC[C@H](C)Oc1cc(Oc2ccc(C(C)=O)cc2)cc(C(=O)Nc2ccn(C)n2)c1
Reaction #48874
desired product
Rendimiento 49.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(=O)c1ccc(-n2c3ccccc3c3ccccc32)cc1
Reaction #66035
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)CC(=O)c1ccc(F)cc1
Reaction #93547
product
Rendimiento 77.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
O=C(CC(=O)c1ccc(F)cc1)c1ccc(F)cc1
Reaction #155740
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)CC1CCN(c2ccc(C(C)=O)cc2)CC1
Reaction #163262
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(CC(=O)C(F)(F)F)c1ccc(F)cc1
Reaction #170442
title compound
Rendimiento 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(=O)c1ccc(N2CCN(C)CC2)cc1
Reaction #177112
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1cccc2cccc(C(=O)C3CCN(C(C)C(=O)c4ccc(F)cc4)CC3)c12
Reaction #197587
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)C(=O)CC(=O)c1ccc(F)cc1
Reaction #199246
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)C(=O)O
Reaction #199731
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)c1ccc(SCCCc2ccccc2)cc1
Reaction #205997
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=CC(=O)c1ccc(F)cc1
Reaction #208972
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)CC1CCN(c2ccc(C(C)=O)cc2)CC1
Reaction #236059
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(CO)c1ccc(F)cc1
Reaction #243451
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1nc(C(=O)N2CCCCC2CC(=O)CC(=O)c2ccc(F)cc2)c(-c2ccc(F)cc2)s1
Reaction #246817
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(=Nc1cccc2c1COC2=O)c1ccc(F)cc1
Reaction #272999
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1ncc2ccc(-c3ccc(F)cc3)nc2n1
Reaction #322060
7-(4-Fluorophenyl)-2-methylpyrido[2,3-d]pyrimidine
Rendimiento 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
CC(=O)c1ccc(SCCCc2ccccc2)cc1
Reaction #346839
p-(3-phenylpropylthio)acetophenone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1977_07
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