fluorobenzene

CC(Cl)C(=O)c1ccc(F)cc1
Reaction #5905
2-chloro-1-(4-fluorophenyl)-1-propanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(=O)N1CCC(C(=O)c2ccc(F)cc2)CC1
Reaction #54971
1-acetyl-4-(p-fluorobenzoyl)piperidine
收率 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
O=C(O)c1ccccc1C(=O)c1ccc(F)cc1
Reaction #63578
2-(4-fluorobenzoyl)benzoic acid
收率 80.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
—
Reaction #63584
intermediate 13
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
O=C1CCC(c2ccc(F)cc2)(c2ccc(F)cc2)CC1
Reaction #63590
4,4-bis(4-fluorophenyl)-1-cyclohexanone
收率 75.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
O=C(c1ccc(F)cc1)c1ccc(Br)cc1
Reaction #64267
4-bromo-4'-fluorobenzophenone
收率 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CC(C)(C#N)c1ccccc1
Reaction #72719
objective compound
收率 50.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(c1ccc(F)cc1)c1ccnc(Cl)c1
Reaction #93803
2-chloro-4-(4-fluorobenzoyl)-pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
CC(=O)Nc1ccc2c(c1)OCCC2(C)C
Reaction #161155
N-(4,4-dimethyl-chroman-7-yl)-acetamide
收率 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CNC(=O)NC(=O)C(CC1CCCC1)c1ccc(-n2nnnc2C)c(C(F)(F)F)c1
Reaction #175666
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(c1ccc(F)cc1)c1ccc(Br)cc1
Reaction #175963
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(c1ccc(F)cc1)c1ccc(Cl)nc1
Reaction #176678
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(c1ccc(F)cc1)c1ccc(Cl)cc1Cl
Reaction #183862
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1CN(Cc2ccc(NS(=O)(=O)c3ccc(-c4ccc(F)cc4)nc3)cc2)CCN1C(=O)OC(C)(C)C
Reaction #184779
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=S(=O)(c1ccc(F)cc1)n1ccc2ccccc21
Reaction #185065
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(c1ccc(OCCN2CCCCC2)cc1)c1c(-c2ccccc2F)ccc2cc(OCc3ccccc3)ccc12
Reaction #186211
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1cc(OC)ccc1-c1ccc(F)cc1
Reaction #192290
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CNC(=O)NC(=O)C(CC1CCCC1)c1ccc(-n2nnnc2C)c(C(F)(F)F)c1
Reaction #195181
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CNC(=O)NC(=O)C(=CC1CCCCC1)c1ccc(S(C)(=O)=O)c(C(F)(F)F)c1
Reaction #207864
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)Nc1ccc(-c2cccc(F)c2)cc1[N+](=O)[O-]
Reaction #209695
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
第 1 页下一页