بحث البنية الفرعية

1268533

COc1ccc2c(c1)CN(c1ccc(OCCN3CCCCC3)cc1)C1=C2CCc2cc(OC)ccc21
Reaction #1809
title compound
المردود 72.4%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(-c2ccc(Cl)cc2)c(-c2ccccc2Cl)[nH]c1=O
Reaction #8901
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)c1oc2nc(-c3ccccc3Cl)c(-c3ccc(Cl)cc3)cc2c1N
Reaction #8902
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(-c2ccc(Cl)cc2)c(-c2ccccc2Cl)[nH]c1=O
Reaction #8904
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(-c2ccc(Cl)cc2)c(-c2ccccc2Cl)nc1OCC(=O)C(C)(C)C
Reaction #8905
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cc(-c2ccc(Cl)cc2)c(-c2ccccc2Cl)nc1OCC(=O)C(C)(C)C
Reaction #8906
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)c1cc2cc(-c3ccc(Cl)cc3)c(-c3ccccc3Cl)nc2o1
Reaction #8910
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(-c2ccc(Cl)cc2)c(-c2ccccc2Cl)[nH]c1=O
Reaction #42091
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(-c2ccc(Cl)cc2)c(-c2ccccc2Cl)nc1Cl
Reaction #42092
2-chloro-6-(2-chlorophenyl)-5-(4-chlorophenyl)pyridine-3-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(-c2ccccc2)[nH]c(=O)c1C(=O)OCC
Reaction #65744
3,4-Diethoxycarbonyl-6-phenyl-2-pyridone
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c([N+](=O)[O-])c(-c2ccccc2)[nH]c(=O)c1C(=O)OCC
Reaction #65745
3,4-Diethoxycarbonyl-5-nitro-6-phenyl-2-pyridone
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(-c2ccc(OCOCCOC)cc2)[nH]c(=O)c1C(=O)OCC
Reaction #65765
3,4-Diethoxycarbonyl-6-(4-methoxyethoxymethoxyphenyl)-2-pyridone
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(O)nc(-c2ccc(OCOCCOC)cc2)c([N+](=O)[O-])c1C(=O)OCC
Reaction #65766
3,4-Diethoxycarbonyl-2-hydroxy-6-(4-methoxyethoxymethoxyphenyl)-5-nitropyridine
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c3c(n(CCCc4cc[nH]n4)c(=O)c2cc1OC)-c1cc2c(cc1C3=O)OCO2
Reaction #160020
solid
المردود 57.6%DOI: 10.6084/m9.figshare.5104873.v1
Nn1c2c(c3ccccc3c1=O)C(=O)c1ccccc1-2
Reaction #160021
solid
المردود 76.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.NCCCCCn1c2c(c3ccccc3c1=O)C(=O)c1ccccc1-2
Reaction #160022
solid
المردود 82.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.NCCCCCCn1c2c(c3ccccc3c1=O)C(=O)c1ccccc1-2
Reaction #160023
solid
المردود 81.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)C(=O)c1c-2n(CCCCl)c(=O)c2ccccc12
Reaction #160025
solid
المردود 17.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1c(-c2ccc(Oc3ccccc3)cc2)[nH]c(=O)c(-c2ccccc2)c1O
Reaction #168236
4-hydroxy-6-oxo-2-(4-phenoxyphenyl)-5-phenyl-1,6-dihydropyridine-3-carbonitrile
المردود 62.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(COC(=O)Nc2ccc(-c3ccccc3)n(CC(=O)NC(C(=O)C(F)(F)C(=O)NCCc3ccccc3)C(C)C)c2=O)n1
Reaction #173021
DOI: 10.1039/C8SC04228D
الصفحة 1التالي