ethyl malonate

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Reaction #1159
Ethoxymagnesium Diethylmalonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)CC(=O)N1CCc2nc(CC)n(Cc3ccc(-c4ccccc4-c4nnn[nH]4)cc3)c2C1C(=O)OCC
Reaction #50147
ethyl 2-ethyl-3-[2'-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl-5-ethoxycarbonylacetyl-4,5,6,7-tetrahydroimidazo[4,5-c]pyridine-4-carboxylate
Rendimiento 67.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CCOC(=O)CC(=O)N1CCc2nc(CC)n(Cc3ccc(-c4ccccc4C(=O)OC(C)(C)C)cc3)c2C1C(=O)OCC
Reaction #50151
ethyl 2-ethyl-3-[2'-(t-butoxycarbonyl)biphenyl-4-yl]methyl-5-ethoxycarbonylacetyl-4,5,6,7-tetrahydroimidazo[4,5-c]pyridine-4-carboxylate
Rendimiento 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
CC(=O)Cc1ccc([N+](=O)[O-])cc1
Reaction #51527
4-nitrophenylacetone
Rendimiento 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC(=O)Cc1ccc([N+](=O)[O-])cc1
Reaction #51528
4-nitrophenylacetone
Rendimiento 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCOC(=O)c1c(N)sc(-c2ccc([N+](=O)[O-])cc2)c1C
Reaction #51529
ethyl 2-amino-4-methyl-5-(4-nitrophenyl)thiophene-3-carboxylate
Rendimiento 63.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCOC(=O)C(C(=O)OCC)C(=O)c1c(F)cc(Cl)c(F)c1Cl
Reaction #64986
diethyl (2,4-dichloro-3,6-difluorobenzoyl)-malonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCOC(=O)/C=C/c1cc(C)c(C(=O)OCC)[nH]1
Reaction #159955
title compound
Rendimiento 47.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)C(C(=O)OCC)c1ncc([N+](=O)[O-])cc1I
Reaction #164912
product
Rendimiento 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)CC(=O)Nc1ccc(Cl)cc1
Reaction #173971
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)CC(=O)Nc1ccc(-c2ccccc2)cc1
Reaction #185100
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)CC(=O)c1ccccc1F
Reaction #193658
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)CC(N)c1ccc(Cl)cc1
Reaction #195857
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)CC(=O)c1cc(Cc2cccc(Cl)c2F)c(OC)cc1F
Reaction #196168
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)CC(=O)c1ccc(Cl)cc1
Reaction #196857
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)CC(=O)c1cccs1
Reaction #205278
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCC(C)(C)CC(=O)CC(=O)OCC
Reaction #206858
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)CC(=O)c1ccc(Br)cc1Cl
Reaction #209502
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)CC(=O)CCCCCNC(=O)OCc1ccccc1
Reaction #212367
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)C=Cc1ccc(OC)nc1
Reaction #214375
ethyl 3-(6-methoxy-3-pyridyl)acrylate
Rendimiento 79.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
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