部分構造検索

COC(=O)c1ccc(N)c(O)c1

CCOC(=O)c1cc(F)c(N2CCC(NC(=O)OC(C)(C)C)C2)c(OC)c1F
Reaction #10380
title compound
収率 77.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCCNc1cc(C(=O)OC)ccc1[N+](=O)[O-]
Reaction #42475
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#CCCN1CCC(COC(=O)c2cc(Cl)c(N)c3c2OCCO3)CC1
Reaction #81914
title compound
収率 17.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)CCN1CCC(COC(=O)c2cc(Cl)c(N)c3c2OCCO3)CC1
Reaction #81915
title compound
収率 41.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(OC(C)C)c(N)c(OC(C)C)c1
Reaction #91027
methyl 4-amino-3,5-diisopropoxybenzoate
収率 74.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(OC(C)C)c(Cl)c(OC(C)C)c1
Reaction #91028
methyl 4-chloro-3,5-diisopropoxybenzoate
収率 36.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(N(C=O)CC(C)=O)c(OC)c1
Reaction #158318
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(-n2cnc(C)c2)c(OC)c1
Reaction #158319
title compound
収率 52.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(=O)O)ccc1-n1cnc(C)c1
Reaction #158320
title compound
収率 53.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(-n2cnc(Br)c2)c(OC)c1
Reaction #158376
title compound
収率 16.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(-n2cnc(Br)c2)c(OC)c1
Reaction #158378
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(=O)NN)ccc1-n1cnc(Cl)c1
Reaction #158379
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(=O)OCc2ccccc2)c(Cl)cc1Nc1ncc(Cl)c(Oc2cccc3c2C(=O)N(C)C3)n1
Reaction #168537
benzyl 2-chloro-4-[5-chloro-4-(2-methyl-3-oxo-2,3-dihydro-1H-isoindol-4-yloxy)-pyrimidin-2-ylamino]-5-methoxy-benzoate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(=O)O)c(Cl)cc1Nc1ncc(Cl)c(Oc2cccc3c2C(=O)N(C)C3)n1
Reaction #168538
2-chloro-4-[5-chloro-4-(2-methyl-3-oxo-2,3-dihydro-1H-isoindol-4-yloxy)-pyrimidin-2-ylamino]-5-methoxy-benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCc1cccc(CC)c1NC(=O)c1nn(C)c2c1CCc1cnc(Nc3ccc(C(=O)O)cc3OC)nc1-2
Reaction #169139
title compound
収率 99.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc([N+](=O)[O-])c(O)c1
Reaction #173008
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc(NC(C)=O)c(O)c1
Reaction #180824
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc(N)c(OC)c1
Reaction #181538
DOI: 10.1039/C8SC04228D
Nc1cc2c(cc1Oc1ccccc1)C(=O)OC2
Reaction #182081
DOI: 10.1039/C8SC04228D
COC(=O)c1cc(OC)c(NC(=O)Oc2ccc([N+](=O)[O-])cc2)cc1C(F)(F)F
Reaction #189324
DOI: 10.1039/C8SC04228D
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