4-oxo-4-phenylbutanoic acid

O=C1CC(C(=O)c2ccccc2)CO1
Reaction #8290
4-benzoyl-dihydro-furan-2-one
Ausbeute 84.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(CCC(=O)N1CC[C@@H]2[C@@H](C1)c1ccccc1N2c1ccccc1)c1ccccc1
Reaction #56190
trans-2-[(3-benzoyl)propionyl]-5-phenyl-2,3,4,4a,5,9b-hexahydro-1H-pyrido[4,3-b]indole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
O=C(O)CCC(=NO)c1ccccc1
Reaction #60736
4-Hydroximino-4-phenylbutyric acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=C1CC[C@@H](c2ccccc2)O1
Reaction #65815
(S)-4-phenyl-γ-butyrolactone
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
Cc1ccc(S(=O)(=O)NC(=O)NCCc2ccc(-n3c(CCC(=O)c4ccccc4)nc4c(C)cc(C)nc43)cc2)cc1
Reaction #78722
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCc1csc([C@H](Cc2ccc([N+](=O)[O-])cc2)NC(=O)CCC(=O)c2ccccc2)n1
Reaction #88319
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCc1csc(C(Cc2ccc([N+](=O)[O-])cc2)NC(=O)CCC(=O)c2ccccc2)n1
Reaction #173032
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)CCC(=O)c1ccccc1
Reaction #223551
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
OCCCC(O)c1ccccc1
Reaction #347362
6a
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_06
CCc1csc(C(Cc2ccc([N+](=O)[O-])cc2)NC(=O)CCC(=O)c2ccccc2)n1
Reaction #404176
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCc1csc([C@H](Cc2ccc([N+](=O)[O-])cc2)NC(=O)CCC(=O)c2ccccc2)n1
Reaction #422205
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CC(C)(C)OC(=O)CCC(=O)c1ccccc1
Reaction #465130
t-butyl 3-benzoylpropionate
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_02
COC(=O)CCC(=O)c1ccccc1
Reaction #465131
methyl 3-benzoylpropionate
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_02
CCc1csc([C@H](Cc2ccc([N+](=O)[O-])cc2)NC(=O)CCC(=O)c2ccccc2)n1
Reaction #512063
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
CCc1csc([C@H](Cc2ccc([N+](=O)[O-])cc2)NC(=O)CCC(=O)c2ccccc2)n1
Reaction #596318
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
—
Reaction #703954
4-methyl- and 4,5-dimethyl-2-phenyl-1,3-dithiolane-2-propionic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_02
O=C(O)CCC(=NO)c1ccccc1
Reaction #756841
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
O=C(CCC(=O)c1ccccc1)OCc1cccc(Oc2ccccc2)c1
Reaction #780519
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCc1csc([C@H](Cc2ccc([N+](=O)[O-])cc2)NC(=O)CCC(=O)c2ccccc2)n1
Reaction #792719
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
Cc1ccc(S(=O)(=O)NC(=O)NCCc2ccc(-n3c(CCC(=O)c4ccccc4)nc4c(C)cc(C)nc43)cc2)cc1
Reaction #811311
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_11
Seite 1Weiter