#5944728

CC(=O)C=Cc1ccc(C)cc1
Reaction #5660
p-methylbenzalacetone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCCC(=O)C1C(=O)CC(C2CCCCC2)CC1=O
Reaction #5661
2-butyryl-5-cyclohexylcyclohexane-1,3-dione
Ausbeute 84.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCCCCCC(C(=O)OC)C(=O)OC
Reaction #5719
dimethyl n-hexylmalonate
Ausbeute 78.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COC(=O)C(C(=O)OC)c1c(-c2ccccc2)c(C)c(C#N)c2nc(C3CC3)oc12
Reaction #45861
compound
Ausbeute 77.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)c1cccc([N+](=O)[O-])c1C(C(=O)OC)C(=O)OC
Reaction #52593
dimethyl 2-methoxycarbonyl-6-nitrophenylmalonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COC(=O)C(C(=O)OC)c1ccc(-c2ccccc2)cc1[N+](=O)[O-]
Reaction #52600
dimethyl-3-nitrobiphenyl-4-malonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COC(=O)c1cccc([N+](=O)[O-])c1C(C(=O)OC)C(=O)OC
Reaction #52719
dimethyl 2-methoxycarbonyl-6-nitrophenylmalonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COC(=O)C(C(=O)OC)c1ccc(-c2ccccc2)cc1[N+](=O)[O-]
Reaction #52740
dimethyl-3-nitrobiphenyl-4-malonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COC(=O)C(C(=O)OC)c1ccc(-c2ccccc2OC)cc1[N+](=O)[O-]
Reaction #52797
dimethyl 2′-methoxy-3-nitrobiphenyl-4-malonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COC(=O)C(C(=O)C=CC(C)Oc1ccc(Oc2ccc(Cl)cc2Cl)cc1)C(=O)OC
Reaction #63426
faint yellow crystalline desired compound
Ausbeute 79.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
COC(=O)C(C(=O)OC)=C1SC=C[SH]1O
Reaction #65192
dimethyl 3-hydroxy-1,3-dithiol-2-ylidenemalonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
COC(=O)C(C(=O)OC)c1ccc(-c2ccccc2)cc1[N+](=O)[O-]
Reaction #77402
dimethyl-3-nitrobiphenyl-4-malonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COC(=O)C(C(=O)OC)c1ccc(-c2ccccc2OC)cc1[N+](=O)[O-]
Reaction #77405
dimethyl 2′-methoxy-3-nitrobiphenyl-4-malonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCOc1ncccc1C1(C(C(=O)OC)C(=O)OC)C(=O)Nc2cc(F)c(Cl)cc21
Reaction #85479
title compound
Ausbeute 38.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COC(=O)C(C(=O)OC)c1ccc([N+](=O)[O-])cn1
Reaction #91689
dimethyl 2-(5-nitropyridin-2-yl)malonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COC(=O)C(C(=O)OC)c1ccc(Br)cc1[N+](=O)[O-]
Reaction #91946
1,3-dimethyl 2-(4-bromo-2-nitrophenyl)propanedioate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
C=C(Br)CC(C(=O)OC)C(=O)OC
Reaction #160609
titled product
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCCCCC1C(=O)CCC1C(C(=O)OC)C(=O)OC
Reaction #180087
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)C(C(=O)OC)C(=O)C(C)Oc1ccc(Oc2ccc(C(F)(F)F)cc2)cc1
Reaction #180960
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)C(C(=O)OC)c1cc(OC)ccc1[N+](=O)[O-]
Reaction #186639
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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