部分構造検索

COc1ccc(CC(=O)O)cc1OC

COCCOCOc1cc(C(ON=C(C(=O)O)c2csc(NC(c3ccccc3)(c3ccccc3)c3ccccc3)n2)C(=O)OC(c2ccccc2)c2ccccc2)cc(F)c1OCOCCOC
Reaction #2671
expected product
収率 56.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Cc1cnc(Cl)nc1Cl)c1ccc(OC)c(OC)c1
Reaction #11885
3-(2,4-dichloro-pyrimidin-5-yl)-2-(3,4-dimethoxy-phenyl)-propionic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Cc1cnc(Nc2ccccc2)nc1Nc1ccccc1)c1ccc(OC)c(OC)c1
Reaction #11886
3-(2,4-diphenylamino-pyrimidin-5-yl)-2-(3,4-dimethoxy-phenyl)-propionic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C2Cc3cnc(Nc4ccccc4)nc3N(c3ccccc3)C2=O)cc1OC
Reaction #11887
6-(3,4-dimethoxy-phenyl)-8-phenyl-2-phenylamino-5,8-dihydro-6H-pyrido[2,3-d]pyrimidin-7-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CC(=O)OCc2ccccc2)cc1OC
Reaction #51859
title compound
収率 60.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CC(=O)OCc2ccccc2)c(S(=O)(=O)N2CCOCC2)cc1OC
Reaction #51860
title compound
収率 60.2%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC(C(=O)OCc1ccccc1)c1cc(OC)c(OC)cc1S(=O)(=O)N1CCOCC1
Reaction #51861
title compound
収率 99.4%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC(C(=O)O)c1cc(OC)c(OC)cc1S(=O)(=O)N1CCOCC1
Reaction #51862
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(C)(C)C(=O)O)ccc1OC(C)C
Reaction #90092
2-(4-Isopropoxy-3-methoxy-phenyl)-2-methyl-propionic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cc(C(Nc2ccc(C(=N)NC(=O)OCc3ccccc3)cc2)C(=O)O)ccc1OC(C)C
Reaction #177298
DOI: 10.1039/C8SC04228D
CCOC(=O)Cc1ccc(OC)c(Oc2ccc(NC(=O)NCc3ccccc3)cc2CN2CCOC2=O)c1
Reaction #178486
DOI: 10.1039/C8SC04228D
COc1ccc(CC(=O)NCCc2ccccc2)cc1OC
Reaction #179797
DOI: 10.1039/C8SC04228D
CCOC(=O)Cc1ccc(OC)c(Oc2ccc(NS(=O)(=O)c3ccc(Cl)cc3)cc2CN2CCOC2=O)c1
Reaction #180292
DOI: 10.1039/C8SC04228D
CCCOc1c(OC)cc(C(C#N)C(=O)OCC)cc1SC
Reaction #182015
DOI: 10.1039/C8SC04228D
CCOC(=O)Cc1ccc(OC)c(Oc2ccc(Br)cc2CN2CCN(C)C2=O)c1
Reaction #182627
DOI: 10.1039/C8SC04228D
CCOC(=O)C(Nc1ccc(C(N)=NC(=O)Nc2ccccc2)cc1)c1cc(OCC)c(OCCO)cc1F
Reaction #189217
DOI: 10.1039/C8SC04228D
CCOC(=O)C(C)c1ccc(OC)c(Oc2ccc(C(F)(F)F)cc2CN2C(=O)OC(c3ccccc3)C2C)c1
Reaction #193991
DOI: 10.1039/C8SC04228D
CCOC(=O)Cc1ccc(OC)c(Oc2ccc([N+](=O)[O-])cc2CN(CC)C(=O)OCc2ccccc2)c1
Reaction #204490
DOI: 10.1039/C8SC04228D
CCN(Cc1cc(Br)ccc1Oc1cc(CC(=O)OC)ccc1OC)C(C)=O
Reaction #212813
DOI: 10.1039/C8SC04228D
CCOC(=O)Cc1ccc(OC)c(Oc2ccc(Cl)cc2CO)c1
Reaction #212910
DOI: 10.1039/C8SC04228D
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