Busqueda de Subestructura

621433

CCOC(=O)C(C(=O)OCC)C(=O)c1c(F)cc(F)c(F)c1C
Reaction #1370
diethyl 2-methyl-3,4,6-trifluorobenzoylmalonate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC(=O)c1c(F)cc(F)c(F)c1C
Reaction #1371
ethyl 2-methyl-3,4,6-trifluorobenzoylacetate
Rendimiento 82.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C(=O)OCC)C(=O)c1cc(F)c(Cl)c([N+](=O)[O-])c1Cl
Reaction #4360
diethyl (2,4-dichloro-5-fluoro-3-nitro-benzoyl)-malonate
Rendimiento 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)C(O)[C@H]1O[C@@H](Oc2n[nH]c(C)c2Cc2ccc(-c3ccccn3)cc2)[C@@](O)(C(C)=O)[C@](O)(C(C)=O)[C@@]1(O)C(C)=O
Reaction #7479
5-Methyl-4-{[4-(pyridin-2-yl)phenyl]methyl}-3-(2,3,4,6-tetraacetyl-β-D-glucopyranosyloxy)-1H-pyrazole
DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc2c(c1O)Cc1cccc3c1[C@@H]2CNC3
Reaction #8808
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C(=O)OCC)C(=O)c1cc(F)c(Cl)c([N+](=O)[O-])c1Cl
Reaction #62802
diethyl(2,4-dichloro-5-fluoro-3-nitrobenzoyl)malonate
Rendimiento 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C(=O)OCC)C(=O)C(C)Oc1ccc(Oc2ccc(C#N)cc2)cc1
Reaction #63423
desired compound
Rendimiento 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C(=O)OCC)C(=O)C(C)Oc1ccc(Oc2ccc(C#N)cc2)cc1
Reaction #63424
desired compound
Rendimiento 86.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C(=O)C=CC(C)Oc1ccc(Oc2ccc(Cl)cc2Cl)cc1)C(=O)OC
Reaction #63426
faint yellow crystalline desired compound
Rendimiento 79.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1C2CCN(CC2)C1Cc1cccnc1)c1cc2ccccc2o1
Reaction #73561
white powder
Rendimiento 50.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2CCN(CC2)[C@H]1Cc1cccnc1
Reaction #73563
(2S)-2-((3-pyridinyl)methyl)-1-azabicyclo[2.2.2]octan-3-one
Rendimiento 96.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C(=O)[C@@](O)(C(=O)O)[C@](O)(C(=O)O)C(=O)c2ccc(C)cc2)cc1.N[C@@H]1C2CCN(CC2)[C@H]1Cc1cccnc1
Reaction #73564
(2S,3R)-3-amino-2-((3-pyridinyl)methyl)-1-azabicyclo[2.2.2]octane di-p-toluoyl-D-tartrate salt
Rendimiento 58.1%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@H]1C2CCN(CC2)[C@H]1Cc1cccnc1
Reaction #73565
(2S,3R)-3-amino-2-((3-pyridinyl)methyl)-1-azabicyclo[2.2.2]octane
Rendimiento 98.1%DOI: 10.6084/m9.figshare.5104873.v1
CC1=Nc2ccc(CC(=O)O)cc2C1(CO)CO
Reaction #77177
(3,3-dihydroxymethyl-2-methyl-3-H-indol-5-yl)-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1C2CCN(CC2)C1Cc1cccnc1)c1cc2ccccc2o1
Reaction #169606
white powder
Rendimiento 55.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1C2CCN(CC2)C1Cc1cccnc1)c1cc2ccccc2o1
Reaction #169607
white powder
Rendimiento 50.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2CCN(CC2)[C@H]1Cc1cccnc1
Reaction #169609
(2S)-2-((3-pyridinyl)methyl)-1-azabicyclo[2.2.2]octan-3-one
Rendimiento 96.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C(=O)[C@@](O)(C(=O)O)[C@](O)(C(=O)O)C(=O)c2ccc(C)cc2)cc1.N[C@@H]1C2CCN(CC2)[C@H]1Cc1cccnc1
Reaction #169610
(2S,3R)-3-amino-2-((3-pyridinyl)methyl)-1-azabicyclo[2.2.2]octane di-p-toluoyl-D-tartrate salt
Rendimiento 58.1%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@H]1C2CCN(CC2)[C@H]1Cc1cccnc1
Reaction #169611
(2S,3R)-3-amino-2-((3-pyridinyl)methyl)-1-azabicyclo[2.2.2]octane
Rendimiento 98.1%DOI: 10.6084/m9.figshare.5104873.v1
CN1C[C@@H]2CNC(=O)c3cc(Cl)ccc3[C@H]2C1
Reaction #172134
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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