ethyl oxalate

COC(=O)C(=O)C=C([O-])c1c(OC)cccc1OC.[Na+]
Reaction #1177
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)C(=O)c1c(-c2ccc(C)cc2)nc2ccc(C)cn12
Reaction #255071
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)C(=O)C(C)c1ccccc1
Reaction #269626
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)C(=O)C=C([O-])c1c(OC)cccc1OC.[Na+]
Reaction #347078
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_06
CCOC(=O)C(=O)C(C#N)c1ccccc1
Reaction #354936
ethyl 3-cyano-3-phenylpyruvate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1976_03
CCOC(=O)C(=O)C(C#N)c1ccccc1
Reaction #355647
ethyl 3-cyano-3-phenylpyruvate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1976_03
CCOC(=O)C(=O)C(C#N)c1ccccc1
Reaction #355653
ethyl 3-cyano-3-phenylpyruvate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1976_03
CCOC(=O)C(=O)C(C)c1ccccc1
Reaction #411853
ethyl (RS)-2-oxo-3-phenylbutyrate
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
CCOC(=O)C(=O)c1ccccc1COC(C)OCC
Reaction #429356
ethyl 2-[2-{(1-ethoxyethyl)oxymethyl}phenyl]-2-oxoacetate
Ausbeute 68.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
CCOC(=O)c1cnc2c(n1)CCCC2
Reaction #472704
ethyl 5,6,7,8-tetrahydroquinoxaline-2-carboxylate
Ausbeute 22.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
O=C(O)C(=O)c1ccncc1
Reaction #629352
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_04
O=C(O)C(=O)c1cccnc1
Reaction #629353
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_04
COC(=O)C(=O)C=C([O-])c1c(OC)cccc1OC.[Na+]
Reaction #652989
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_01
CCOC(=O)C(=O)C=C([O-])c1c(OC)cccc1OC.[K+]
Reaction #652990
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_01
COC(=O)C(=O)C=C([O-])c1c(OC)cccc1OC.[Na+]
Reaction #669937
expected product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_07
O=C(O)C(=O)CCc1ccccc1
Reaction #708356
2-oxo-4-phenylbutyric acid
Ausbeute 90.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1989_04
CCOC(=O)C(=O)[O-]
Reaction #756577
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCOC(=O)C(=O)N1C(C)CN(c2c(F)cc3c(=O)c(C(=O)NCc4ccc(Cl)cc4Cl)cn(CC(F)(F)F)c3c2OC)CC1C
Reaction #788848
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CCN1C(=O)C(O)=C(c2ccccc2)S1(=O)=O
Reaction #816427
title compound
Ausbeute 2754.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
CCCCN1C(=O)C(O)=C(c2ccc(Cl)cc2)S1(=O)=O
Reaction #816437
title compound
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_09
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