ethyl potassium malonate

O=C([O-])CC(=O)[O-].[CH2]C.[Mg+2]
Reaction #302879
Ethyl Magnesium Malonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CCOC(=O)CC(=O)CCN(Cc1ccc(Cl)cc1)C(=O)C1(C)CCN1C(=O)Cc1cc(C)cc(C)c1
Reaction #495790
5-((4-chloro-benzyl)-{1-[2-(3,5-dimethyl-phenyl)-acetyl]-2-methyl-azetidine-2-carbonyl}-amino)-3-oxo-pentanoic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
CCOC(=O)CC(=O)c1cccc2ccccc12
Reaction #498306
3-Naphthalen-1-yl-3-oxo-propionic acid ethyl ester
Ausbeute 66.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
CCOC(=O)CC(=O)O
Reaction #632148
monoethyl hydrogen malonate
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
CCOC(=O)CC(=O)O
Reaction #975155
monoethyl hydrogen malonate
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
CCOC(=O)CC(=O)c1ccc(-n2c(C)nc3cnccc32)nc1
Reaction #979964
title compound
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_06
CCOC(=O)CC(=O)c1ccc(-n2c(C)nc3cnccc32)nc1
Reaction #1060674
title compound
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_11
CCOC(=O)CC(=O)c1ccnc(-c2ccccc2)n1
Reaction #1132855
3-oxo-3-(2-phenyl-pyrimidin-4-yl)-propionic acid ethyl ester
Ausbeute 58.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
CCOC(=O)CC(=O)[C@@H](COCc1ccccc1)NC(=O)OC(C)(C)C
Reaction #1143295
title compound
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_07
CCOC(=O)CC(=O)C(C)(C)NC(=O)OC(C)(C)C
Reaction #1143522
title compound
Ausbeute 17.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_07
CCOC(=O)CC(=O)O
Reaction #1179916
monoethyl hydrogen malonate
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
c1ccc2[nH]ccc2c1
Reaction #1182698
Indole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
O=C([O-])CC(=O)[O-].[CH2]C.[Mg+2]
Reaction #1244281
Ethyl Magnesium Malonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_10
CCOC(=O)CC(=O)CC(c1ccccc1)c1ccccc1
Reaction #1285215
desired product
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_01
CCOC(=O)CC(=O)C1(c2ccccc2)CCCC1
Reaction #1285218
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_01
CCOC(=O)CC(=O)CCCCCCCCCCCOC1CCCCO1
Reaction #1285222
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_01
CCCCCCCCCCCCS(=O)(=O)CCCC(=O)CC(=O)OCC
Reaction #1285238
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_01
CCOC(=O)CC(=O)c1cccc2ccccc12
Reaction #1352460
3-Naphthalen-1-yl-3-oxo-propionic acid ethyl ester
Ausbeute 66.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_04
CCOC(=O)CC(=O)c1ncccc1F
Reaction #1584850
3-(3-Fluoro-pyridin-2-yl)-3-oxo-propionic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_12
CCOC(=O)CC(=O)c1nccnc1Cl
Reaction #1584857
3-(3-Chloro-pyrazin-2-yl)-3-oxo-propionic acid ethyl ester
Ausbeute 39.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_12
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