子结构搜索

14918

CC1(C)C(=O)Nc2ccc(-c3ccc(F)c(Cl)c3)cc21
Reaction #7104
title compound
收率 30.0%DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc2nc(-c3ccc(O)c(F)c3)cc(-c3ccc(F)cc3)c2c1
Reaction #7343
2-(3-Fluoro-4-hydroxyphenyl)-4-(4-fluorophenyl)quinolin-6-ol
收率 90.0%DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc(-c2nc3ccc(O)cc3c(-c3ccc(F)cc3)c2Cl)cc1
Reaction #7350
3-Chloro-4-(4-fluorophenyl)-2-(4-hydroxyphenyl)quinolin-6-ol
收率 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC[C@H]1O[C@@H](Oc2n[nH]c(C)c2Cc2ccc(-c3ccc(F)cc3)cc2)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #7471
4-{[4-(4-fluorophenyl)phenyl]methyl}-5-methyl-3-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)-1H-pyrazole
收率 60.1%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(-c2nccc3ccccc23)c(F)c1
Reaction #8651
1-(2,4-difluoro-phenyl)-isoquinoline
DOI: 10.6084/m9.figshare.5104873.v1
CCOC1=C(c2ccc(F)cc2)C(=O)CC1
Reaction #9370
3-ethoxy-2-(4-fluoro-phenyl)-cyclopent-2-enone
收率 70.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(-c2ccc3c(c2)C2(CCCCC2)C(=NOCc2ccccc2)N3)cc1
Reaction #9428
desired product
收率 67.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(-c2ccc3c(c2)C2(CCCCC2)C(=NOCc2ccccc2)N3)cc1F
Reaction #9429
desired product
收率 69.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2c(cnn2-c2ccc(F)cc2)cc1I
Reaction #41344
subtitle compound
收率 51.1%DOI: 10.6084/m9.figshare.5104873.v1
OB(O)c1ccc(F)cc1OC1CCCCO1
Reaction #41919
4-Fluoro-2-(tetrahydropyran-2-yloxy)benzeneboronic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cscc1NC(=O)COc1ccc(-c2ccc(F)cc2)cc1
Reaction #42868
title compound
收率 124.3%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cc(-c2ccnc(Cl)n2)ccc1F
Reaction #43147
5-(2-Chloro-pyrimidin-4-yl)-2-fluoro-benzaldehyde
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cc(-c2ccnc(Cl)n2)ccc1F
Reaction #43258
5-(2-chloropyrimidin-4-yl) 2-fluorobenzaldehyde
收率 40.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cccc(-c2ccc(F)cc2)n1
Reaction #43801
desired product
收率 46.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(Oc2ccc3c(c2)cc(C(=O)N2CCC(F)(F)CC2)n3-c2ccc(F)cc2)CC1
Reaction #48131
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(Oc2ccc3c(c2)cc(C(=O)N2CCC(F)(F)CC2)n3-c2ccc(F)c(C#N)c2)CC1
Reaction #48150
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(Oc2ccc(F)cc2)cc1
Reaction #51654
4-(4-fluorophenoxy)benzoic acid
收率 91.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC1=C(c2ccc(F)cc2)C(=O)CC1
Reaction #57012
3-ethoxy-2-(4-fluoro-phenyl)-cyclopent-2-enone
收率 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CSc1nc(-c2ccccc2C)c2ccc(=O)n(-c3c(F)cccc3F)c2n1
Reaction #58365
title compound
收率 63.0%DOI: 10.6084/m9.figshare.5104873.v1
O=CN1CCN(c2ccc(-c3ccc(F)cc3)cn2)CC1
Reaction #60670
title product
收率 94.7%DOI: 10.6084/m9.figshare.5104873.v1
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