6b

C[Si](C)(C)C#Cc1cc(-c2ccc(O)c(F)c2)nc2ccc(O)cc12
Reaction #7338
2-(3-Fluoro-4-hydroxyphenyl)-4-[(trimethylsilyl)ethynyl]quinolin-6-ol
المردود 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Oc1ccc2nc(-c3ccc(O)c(F)c3)cc(C#Cc3ccccc3)c2c1
Reaction #7340
2-(3-Fluoro-4-hydroxyphenyl)-4-(phenylethynyl)quinolin-6-ol
المردود 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Oc1ccc2nc(-c3ccc(O)c(F)c3)cc(-c3nccs3)c2c1
Reaction #7341
2-(3-Fluoro-4-hydroxyphenyl)-4-thiazol-2-yl-quinolin-6-ol
المردود 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1ccc(-c2cc(-c3ccc(O)c(F)c3)nc3ccc(O)cc23)cc1
Reaction #7342
2-(3-Fluoro-4-hydroxyphenyl)-4-(4-methylphenyl)quinolin-6-ol
المردود 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Oc1ccc2nc(-c3ccc(O)c(F)c3)cc(-c3ccc(F)cc3)c2c1
Reaction #7343
2-(3-Fluoro-4-hydroxyphenyl)-4-(4-fluorophenyl)quinolin-6-ol
المردود 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Oc1ccc2nc(-c3ccc(O)c(F)c3)cc(-c3ccc(Cl)cc3)c2c1
Reaction #7344
4-(4-Chlorophenyl)-2-(3-fluoro-4-hydroxyphenyl)quinolin-6-ol
المردود 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
N#Cc1ccc(-c2cc(-c3ccc(O)c(F)c3)nc3ccc(O)cc23)cc1
Reaction #7345
4-(4-Cyanophenyl)-2-(3-fluoro-4-hydroxyphenyl)quinolin-6-ol
المردود 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Oc1ccc2nc(-c3ccc(O)c(F)c3)cc(-c3ccc(C(F)(F)F)cc3)c2c1
Reaction #7346
2-(3-Fluoro-4-hydroxyphenyl)-4-(4-trifluoromethylphenyl)quinolin-6-ol
المردود 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Oc1ccc2nc(-c3ccc(O)c(F)c3)cc(-c3ccsc3)c2c1
Reaction #7347
2-(3-Fluoro-4-hydroxyphenyl)-4-thiophen-3-yl-quinolin-6-ol
المردود 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Oc1ccc2nc(-c3ccc(O)c(F)c3)cc(-c3ccncc3)c2c1
Reaction #7348
2-(3-Fluoro-4-hydroxyphenyl)-4-(4-pyridinyl)quinolin-6-ol
المردود 20.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Oc1ccc2nc(-c3ccc(O)c(F)c3)cc(-c3cncnc3)c2c1
Reaction #7349
2-(3-Fluoro-4-hydroxyphenyl)-4-(5-pyrimidinyl)quinolin-6-ol
المردود 34.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Oc1ccc2nc(-c3ccc(O)c(F)c3)cc(C#Cc3ccccc3)c2c1
Reaction #173711
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Oc1ccc2nc(-c3ccc(O)c(F)c3)cc(-c3nccs3)c2c1
Reaction #201702
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C[Si](C)(C)C#Cc1cc(-c2ccc(O)c(F)c2)nc2ccc(O)cc12
Reaction #372049
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Oc1ccc2nc(-c3ccc(O)c(F)c3)cc(-c3ccc(F)cc3)c2c1
Reaction #377080
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Oc1ccc2nc(-c3ccc(O)c(F)c3)cc(-c3ccc(C(F)(F)F)cc3)c2c1
Reaction #379232
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Oc1ccc2nc(-c3ccc(O)c(F)c3)cc(-c3cncnc3)c2c1
Reaction #787735
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
Cc1ccc(-c2cc(-c3ccc(O)c(F)c3)nc3ccc(O)cc23)cc1
Reaction #1049415
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
Oc1ccc2nc(-c3ccc(O)c(F)c3)cc(-c3ccsc3)c2c1
Reaction #1221243
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
N#Cc1ccc(-c2cc(-c3ccc(O)c(F)c3)nc3ccc(O)cc23)cc1
Reaction #1655432
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
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