Busqueda de Subestructura

13693

Oc1ccc2nc(-c3ccc(O)c(F)c3)cc(-c3cncnc3)c2c1
Reaction #7349
2-(3-Fluoro-4-hydroxyphenyl)-4-(5-pyrimidinyl)quinolin-6-ol
Rendimiento 34.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cncnc2)cc1C=O
Reaction #10733
2,4-Dimethoxy-5-pyrimidin-5-yl-benzaldehyde
Rendimiento 98.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2cc(C=O)c(OC)cc2OC)c(OC)n1
Reaction #10745
5-(2,4-Dimethoxy-pyrimidin-5-yl)-2,4-dimethoxy-benzaldehyde
Rendimiento 75.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccsc1-c1cnc(OC(C)(C)C)nc1OC(C)(C)C
Reaction #40938
title compound
Rendimiento 32.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2cccc(C)n2)c(OC)n1
Reaction #40959
title compound
Rendimiento 47.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2ccc(C)nc2)c(OC)n1
Reaction #40965
title compound
Rendimiento 62.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2oc(C)nc2C)c(OC)n1
Reaction #40968
title compound
Rendimiento 67.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2cccc(F)n2)c(OC)n1
Reaction #40981
title compound
Rendimiento 57.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2ccc(Cl)nc2)c(OC)n1
Reaction #40992
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2cc(C)cnc2F)c(OC)n1
Reaction #41000
title compound
Rendimiento 33.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2cccnc2C#N)c(OC)n1
Reaction #41004
title compound
Rendimiento 79.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2cnccc2C)c(OC)n1
Reaction #41011
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2ccc(C)nc2F)c(OC)n1
Reaction #41014
title compound
Rendimiento 75.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2cccnn2)c(OC)n1
Reaction #41018
title compound
Rendimiento 34.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2cnccn2)c(OC)n1
Reaction #41021
title compound
Rendimiento 45.4%DOI: 10.6084/m9.figshare.5104873.v1
CN1C[C@H]2CCN(c3ccc(-c4ccc(-c5cncnc5)cc4)cc3)[C@H]2C1
Reaction #41237
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2ccc(-c3ccc(N4CC[C@@H]5CN(C)C[C@@H]54)cc3)cc2)cn1
Reaction #41252
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc([N+](=O)[O-])cc1Nc1cc(-c2cncnc2)ncn1
Reaction #42049
objective compound
Rendimiento 21.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-n2c(C(=O)N3CCC(F)(F)CC3)cc3cc(OC4CCN(C(C)C)CC4)ccc32)cn1
Reaction #48151
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(-c2ccnc3c2cc(-c2cnc(N4CCN(C(=O)OC(C)(C)C)CC4)nc2)n3S(=O)(=O)c2ccccc2)c(-c2ccc([N+](=O)[O-])cc2)n1
Reaction #57284
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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