部分構造検索

COC(=O)C=Cc1cccc(N)c1

COC(=O)CCc1cccc(N)c1
Reaction #45225
3-(3-amino-phenyl)propionic acid methyl ester
収率 98.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=Cc1cc(NN=CC(=O)C(F)(F)F)ccc1Cl
Reaction #76774
ethyl 2-chloro-5-(3,3,3-trifluoro-2-oxopropylidenehydrazino)cinnamate
収率 97.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=Cc1cc(NN)ccc1Cl
Reaction #76775
ethyl 2-chloro-5-hydrazinocinnamate
収率 34.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)=Cc1cccc([N+](=O)[O-])c1
Reaction #95080
title product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C=C/c1ccc2c(c1)N(C)C(=O)C(C)(C)C(=O)N2CC
Reaction #156127
title compound
収率 103.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCc1ccc2c(c1)N(C)C(=O)C(C)(C)C(=O)N2CC
Reaction #156128
title compound
収率 80.1%DOI: 10.6084/m9.figshare.5104873.v1
CCSCCOC(=O)C(Br)=Cc1cc(-n2c(=O)cc(C(F)(F)F)n(C)c2=O)ccc1Cl
Reaction #178591
DOI: 10.1039/C8SC04228D
O=C1OCCC1=Cc1cc(NC(=O)C(F)(F)F)ccc1S(=O)(=O)Nc1ccc2c(c1)B(O)OC2
Reaction #182251
DOI: 10.1039/C8SC04228D
CCOC(=O)C=Cc1cc(-n2cnnc2)cc(C(F)(F)F)c1N
Reaction #183250
DOI: 10.1039/C8SC04228D
CCOC(=O)C(Cl)=Cc1cc(NC(N)=O)ccc1Cl
Reaction #183667
DOI: 10.1039/C8SC04228D
CCOC(=O)C(Cl)=Cc1cc(NC(=O)C2=C(C(N)=O)CCCC2)ccc1Cl
Reaction #188201
DOI: 10.1039/C8SC04228D
CCOC(=O)C=Cc1cccc(NC(=O)c2ccc3oc4ccccc4c3c2)c1
Reaction #189411
DOI: 10.1039/C8SC04228D
CCOC(=O)C=Cc1ccc(Oc2ccc(Cl)cc2Cl)c(NS(C)(=O)=O)c1
Reaction #190745
DOI: 10.1039/C8SC04228D
CCN(CC)CCNc1ccc(C=CC(=O)OC)cc1N
Reaction #190781
DOI: 10.1039/C8SC04228D
CCOC(=O)C(Cl)=Cc1cc(NC(=O)C2=C(C(=O)N(C)C)CCCC2)ccc1Cl
Reaction #191611
DOI: 10.1039/C8SC04228D
CCOC(=O)C=Cc1cc([N+](=O)[O-])ccc1-c1ccc(OC(F)(F)F)cc1
Reaction #200793
DOI: 10.1039/C8SC04228D
COC(=O)C=Cc1cccc(N)c1
Reaction #202504
DOI: 10.1039/C8SC04228D
CCOC(=O)C=Cc1cccc(NC(=O)c2ccc(-c3ccc(-c4ccccc4)c(F)c3)o2)c1
Reaction #206978
DOI: 10.1039/C8SC04228D
Cc1nccn1-c1cccc(C2=CC(=O)OC(C)(C)O2)c1
Reaction #209152
DOI: 10.1039/C8SC04228D
CCOC(=O)C=Cc1cccc(NC(=O)c2ccc(-c3cccc(Cl)c3)o2)c1
Reaction #213591
DOI: 10.1039/C8SC04228D
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