Recherche de Sous-structure

593258

COc1cc(Cl)c(C)cc1-c1ccc(OC(C)C(O)CCc2cccnc2)cc1
Reaction #180742
DOI: 10.1039/C8SC04228D
CC(Oc1ccc(-c2cc(F)c(S(N)(=O)=O)cc2F)cc1)C(O)CCc1cccnc1
Reaction #187954
DOI: 10.1039/C8SC04228D
CC(Oc1ccc(-c2ccc(C#N)c(C#N)c2)cc1)C(O)CCc1cccnc1
Reaction #191492
DOI: 10.1039/C8SC04228D
COc1ccc(C#N)cc1-c1ccc(OC(C)C(O)CCc2cccnc2)cc1
Reaction #193916
DOI: 10.1039/C8SC04228D
Cc1cc(-c2ccc(OC(C)C(O)CCc3cccnc3)cc2)ccc1C#N
Reaction #244193
DOI: 10.1039/C8SC04228D
CC(Oc1ccc(-c2ccc(C#N)c(Cl)c2)cc1)C(O)CCc1cccnc1
Reaction #256202
DOI: 10.1039/C8SC04228D
CC(Oc1ccc(-c2ccc(S(N)(=O)=O)c(F)c2)cc1)C(O)CCc1cccnc1
Reaction #271522
DOI: 10.1039/C8SC04228D
CC(Oc1ccc(-c2ccc(OCCN3CCCC3)cc2)cc1)C(O)CCc1cccnc1
Reaction #391134
DOI: 10.1039/C8SC04228D
C[C@H](Oc1ccc(B(O)O)cc1)C(CCc1cccnc1)O[Si](C)(C)C(C)(C)C
Reaction #467153
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Oc1ccc(B(O)O)cc1)[C@@H](CCc1cccnc1)O[Si](C)(C)C(C)(C)C
Reaction #467160
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)Cc1cccc(-c2ccc(O[C@@H](C)[C@H](O)CCc3cccnc3)cc2)c1
Reaction #467162
title compound
Rendement 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(Oc1ccc(-c2ccc(Cl)cc2)cc1)C(O)CCc1cccnc1
Reaction #467163
4-(4′-Chlorobiphenyl-4-yloxy)-1-pyridin-3-yl-pentan-3-ol
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Oc1ccc(-c2ccc(Cl)cc2Cl)cc1)[C@H](O)CCc1cccnc1
Reaction #467165
solid
Rendement 33.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C#N)ccc1-c1ccc(O[C@@H](C)[C@H](O)CCc2cccnc2)cc1
Reaction #467167
oil
Rendement 83.6%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)Cc1ccc(-c2ccc(O[C@@H](C)[C@H](O)CCc3cccnc3)cc2)cc1
Reaction #467170
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Oc1ccc(-c2cccc(CCN(C)C)c2)cc1)[C@H](O)CCc1cccnc1
Reaction #467173
title compound
Rendement 35.9%DOI: 10.6084/m9.figshare.5104873.v1
CNCCc1ccc(-c2ccc(O[C@@H](C)[C@H](O)CCc3cccnc3)cc2)cc1
Reaction #467176
title compound
Rendement 43.1%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Oc1ccc(-c2cccc(NC(N)=O)c2)cc1)[C@H](O)CCc1cccnc1
Reaction #467177
title compound
Rendement 61.5%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Oc1ccc(-c2ccc(Cl)c(Cl)c2)cc1)[C@H](O)CCc1cccnc1.O=C(O)C(=O)O
Reaction #467178
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Oc1ccc(B(O)O)cc1)[C@H](O)CCc1cccnc1
Reaction #467179
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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