部分構造検索

842

O=C1CN(c2ccc(F)cc2)CCN1
Reaction #437
収率 0.0%
O=C1CN(c2ccc(F)cc2)CCN1
Reaction #438
収率 0.0%
Fc1ccc(N2CCN(Cc3ccccc3)CC2)cc1
Reaction #439
収率 75.0%
CN(C)C(=O)c1cc(C2CCCN2c2ccc(F)cc2)c2oc(N3CCOCC3)cc(=O)c2c1
Reaction #557
収率 15.0%
CN(C)C(=O)c1cc(C2CCCN2c2ccc(F)cc2)c2oc(N3CCOCC3)cc(=O)c2c1
Reaction #558
収率 19.1%
CN(C)C(=O)c1cc(C2CCCN2c2ccc(F)cc2)c2oc(N3CCOCC3)cc(=O)c2c1
Reaction #559
収率 49.5%
CN(C)C(=O)c1cc(C2CCCN2c2ccc(F)cc2)c2oc(N3CCOCC3)cc(=O)c2c1
Reaction #560
収率 16.0%
CN(C)C(=O)c1cc(C2CCCN2c2ccc(F)cc2)c2oc(N3CCOCC3)cc(=O)c2c1
Reaction #561
収率 19.0%
O=C(c1cc(C2CCCN2c2ccc(F)cc2)c2oc(N3CCOCC3)cc(=O)c2c1)N1CCOCC1
Reaction #587
収率 45.6%
CCOC(=O)c1ccc(-c2ccc(F)cc2)cc1
Reaction #5237
title compound
DOI: 10.6084/m9.figshare.5104873.v1
OCCCc1ccc(F)cc1
Reaction #5312
title compound
収率 51.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(F)c(F)c(Cl)c1NC1CC1
Reaction #10398
title compound
収率 63.7%DOI: 10.6084/m9.figshare.5104873.v1
C#CC(C)(O)Cc1ccc(F)cc1
Reaction #42160
(4-fluorophenyl)-2-methyl-3-butyne-2-ol
収率 97.0%DOI: 10.6084/m9.figshare.5104873.v1
C#CC(C)(O)Cc1ccc(F)cc1
Reaction #42179
(4-fluorophenyl)-2-methyl-3-butyne-2-ol
収率 96.7%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cc(Br)c(O)cc1F
Reaction #43942
title compound
収率 81.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccc(F)c(CCN2CCN(c3cccc4nc(C)ccc34)CC2)c1
Reaction #44145
title compound
収率 66.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(N3CCN(CCc4cc(Br)ccc4F)CC3)cccc2n1
Reaction #44146
title compound
収率 95.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(N3CCN(CCc4cc(NC(=O)C(C)(C)C)ccc4F)CC3)cccc2n1
Reaction #44147
title compound
収率 52.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(N3CCN(CCc4cc(NS(C)(=O)=O)ccc4F)CC3)cccc2n1
Reaction #44148
title compound
収率 69.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(N3CCN(CCc4cc(N5CCNC5=O)ccc4F)CC3)cccc2n1
Reaction #44149
title compound
収率 35.0%DOI: 10.6084/m9.figshare.5104873.v1
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