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O=C(O)CC(=O)O

CCc1c(O)nc(-c2ccccc2)[nH]c1=O
Reaction #1539
5-ethyl-6-hydroxy-2-phenyl-4(3H)-pyrimidinone
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(Cc1ccccc1)C(=O)OCC
Reaction #6176
title compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OC(=O)C(c2cccc3nnsc23)C(=O)O1
Reaction #6457
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(CCC(F)=C(F)F)C(=O)O
Reaction #6566
2-(3,4,4-Trifluoro-3-butenyl)malonic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Br)(Oc1cccc2[nH]ccc12)C(=O)OCC
Reaction #44843
7
Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Oc1cccc2[nH]ccc12)C(=O)OCC
Reaction #44844
8
Ausbeute 34.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1[nH]c(C(C)(C)C)cc1N
Reaction #47203
methyl 3-amino-5-tert-butyl-1H-pyrrole-2-carboxylate
Ausbeute 34.0%DOI: 10.6084/m9.figshare.5104873.v1
OCC(CO)Cc1ccccc1
Reaction #49834
2-benzyl-1,3-propanediol
Ausbeute 105.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCc1c(C(=O)OCC)[nH]c2c1CCCC2
Reaction #52776
3-(2-ethoxycarbonylethyl)-4,5,6,7-tetrahydro-1H-indole-2-carboxylic acid ethyl ester
Ausbeute 109.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(C(=O)OCC)CC2CCC2C1
Reaction #54586
3,3-bis(ethoxycarbonyl)bicyclo-[3.2.0]heptane
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1(C(=O)O)CC2CCC2C1
Reaction #54587
bicyclo[3.2.0]heptane-3,3-dicarboxylic acid
Ausbeute 87.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CC)(CCCC1CCCCC1)C(=O)OCC
Reaction #55583
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C(=O)OCC)c1ccc(N)cc1
Reaction #56898
2-(4-amino-phenyl)-malonic acid diethyl ester
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(C(CO)CO)cc1
Reaction #56899
2-(4-amino-phenyl)-propane-1,3-diol
Ausbeute 17.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=Cc1cccc(C2OCCO2)c1)C(=O)OCC
Reaction #58726
Diethyl 2-[(3-(1,3-dioxolan-2-yl)phenyl)methylene]propane-1,3-dioate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1C(=O)Nc2ccc(Cl)cc2CC1c1ccc(OC)cc1
Reaction #63800
title compound
Ausbeute 91.5%DOI: 10.6084/m9.figshare.5104873.v1
C=C(Cc1ccccc1)C(=O)OCC
Reaction #64651
title compound
Ausbeute 85.5%DOI: 10.6084/m9.figshare.5104873.v1
C=C(Cc1ccccc1)C(=O)OCC
Reaction #65022
title compound
Ausbeute 85.5%DOI: 10.6084/m9.figshare.5104873.v1
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.v1
CC(C)OC(=O)C(C(=O)O)=C1SC=CS1
Reaction #65193
isopropyl hydrogen 1,3-dithiol-2-ylidenemalonate
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
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