ethyl pyruvate

CCOC(=O)C(C)Nc1ccc(F)c(F)c1F
Reaction #8529
title compound
수율 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)C(C)Nc1ccc(F)c(F)c1F
Reaction #8531
title compound
수율 97.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)C(C)Nc1ccc(F)c(F)c1F
Reaction #8533
title compound
수율 94.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)C(C)=NNC
Reaction #44233
desired product
수율 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccc2c(n1)NC(C)C(=O)N2
Reaction #49812
desired compound
수율 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
—
Reaction #51289
ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCOC(=O)[C@H](C)Nc1ccc(Cl)c(Cl)c1
Reaction #51300
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCOC(=O)[C@H](C)Nc1ccc(Cl)c(C(F)(F)F)c1
Reaction #51301
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCOC(=O)[C@H](C)Nc1cc(Cl)cc(Cl)c1
Reaction #51302
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCOC(=O)[C@H](C)Nc1ccc(F)c(F)c1
Reaction #51303
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCOC(=O)[C@H](C)Nc1ccc2ccccc2c1
Reaction #51334
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCOC(=O)C(C)=NNc1ccc(Cl)cc1Cl
Reaction #78310
title compound
수율 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCOC(=O)C(C)=NNc1cccc([N+](=O)[O-])c1
Reaction #161096
2-[(3-nitro-phenyl)-hydrazono]-propionic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
—
Reaction #161642
powder
수율 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
—
Reaction #161649
solid
수율 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)C(C)(O)c1ccc2c(Br)c(OC)ccc2c1
Reaction #177353
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)C(C)Nc1ccc(F)c(F)c1F
Reaction #211580
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)[C@H](C)Nc1ccc(Cl)c(Cl)c1
Reaction #220491
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CCOC(=O)[C@H](C)Nc1ccc(Cl)c(C(F)(F)F)c1
Reaction #220492
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CCOC(=O)[C@H](C)Nc1cc(Cl)cc(Cl)c1
Reaction #220493
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
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