methyl benzoyl formate

COC(=O)C(=NO)c1ccccc1
Reaction #188345
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(C(=O)N1CCCCC1)c1ccccc1
Reaction #230763
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC=C(C(=O)OC)c1ccccc1
Reaction #273936
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Oc1nc2ccc(Cl)nc2nc1-c1ccccc1
Reaction #309167
6-chloro-3-phenylpyrido[2,3-b]pyrazin-2-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CN(C)CC#CCN(C=O)C(=O)c1ccccc1
Reaction #379822
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC#CC(O)(C(=O)OC)c1ccccc1
Reaction #445425
Methyl α-Phenyl-α-(1-propynyl)glycolate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1984_08
C/C=C/C(O)(C(=O)OC)c1ccccc1
Reaction #445427
Methyl α-Phenyl-α-(trans-1-propenyl)glycolate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1984_08
Oc1c(-c2ccccc2)sc(-c2ccccc2)c1-c1ccccc1
Reaction #446331
3-Hydroxy-2,4,5-triphenylthiophene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_03
COC(=O)C(O)(c1ccccc1)C1CCCC1
Reaction #464967
methyl 2-phenyl-2-cyclopentyl-2-hydroxy-acetate
Yield 76.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_02
CCCCCCOC(=O)C(=O)c1ccccc1
Reaction #480319
hexyl phenylglyoxalate
Yield 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_10
COC(=O)C(=NO)c1ccccc1
Reaction #480321
methyl α-(hydroxyimino)-2-phenylacetate
Yield 100.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_10
CO/C=C(/C(=O)OC)c1ccccc1
Reaction #500683
E-methyl 3-methoxy-2-phenylpropenoate
Yield 50.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
C=C(C(=O)OC)C1=CC=CC(=S(=O)=O)C1c1ccccc1
Reaction #527561
2-phenyl-3-sulfonylphenyl-propenoic acid, methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_05
COC(=O)/C(=N/O)c1ccccc1
Reaction #671526
methyl E-2-hydroxyimino-2-phenylacetate
Yield 13.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_08
COc1ccccc1C(O)(C(=O)O)c1ccccc1
Reaction #747256
Hydroxy-(2-methoxy-phenyl)-phenyl-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
CC=CC(O)(C(=O)OC)c1ccccc1
Reaction #784453
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
O=C(C(=O)N1CCCCC1)c1ccccc1
Reaction #978407
1-(phenylglyoxylyl)piperidine
Yield 96.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_02
CN(C)CC#CCN(C=O)C(=O)c1ccccc1
Reaction #1061180
N-(4-dimethylamino-2-butynyl)benzoylformamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_11
CO/C=C(/C(=O)OC)c1ccccc1
Reaction #1121543
E-methyl 3-methoxy-2-phenylpropenoate
Yield 50.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_05
COC(=O)/C(=N/O)c1ccccc1
Reaction #1157211
methyl E-2-hydroxyimino-2-phenylacetate
Yield 13.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_06
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