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645919

O=C(O[C@H]1Cc2c(O)cc(O)cc2O[C@H]1c1cc(O)c(O)c2c(O)c(=O)cc([C@H]3Oc4cc(O)cc(O)c4C[C@H]3O)cc12)c1cc(O)c(O)c(O)c1
Reaction #8611
theaflavin 3-gallate
Ausbeute 28.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O[C@@H]1Cc2c(O)cc(O)cc2O[C@@H]1c1cc(=O)c(O)c2c(O)c(O)cc([C@H]3Oc4cc(O)cc(O)c4C[C@H]3OC(=O)c3cc(O)c(O)c(O)c3)c2c1)c1cc(O)c(O)c(O)c1
Reaction #8612
theaflavin 3,3′-digallate
Ausbeute 10.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O[C@@H]1Cc2c(O)cc(O)cc2O[C@@H]1c1cc(=O)c(O)c2c(O)c(O)cc([C@@H]3Oc4cc(O)cc(O)c4C[C@@H]3O)c2c1)c1cc(O)c(O)c(O)c1
Reaction #8616
compound 3
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2cn([C@H]3CC[C@H](N4CCNCC4C)CC3)c3ncnc(Cl)c23)ccc1Oc1ccccc1
Reaction #79850
title compound
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1
Clc1cc(Br)ccc1Oc1ccccc1
Reaction #79853
4-Bromo-2-chloro-1-phenoxybenzene
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OB(c2ccc(Oc3ccccc3)c(Cl)c2)OC1(C)C
Reaction #79854
title compound
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN([C@H]2CC[C@H](n3cc(-c4ccc(Oc5ccccc5)c(Cl)c4)c4c(N)ncnc43)CC2)CC1
Reaction #79855
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc(Br)ccc1Oc1ccccc1
Reaction #79856
title compound
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OB(c2ccc(Oc3ccccc3)c(F)c2)OC1(C)C
Reaction #79857
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN([C@H]2CC[C@H](n3cc(-c4ccc(Oc5ccccc5)c(F)c4)c4c(Cl)ncnc43)CC2)CC1
Reaction #79858
title compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Br)ccc1Oc1ccccc1
Reaction #79859
title compound
Ausbeute 35.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2cn([C@H]3CC[C@H](N4CCN(C)CC4)CC3)c3ncnc(Cl)c23)ccc1Oc1ccccc1
Reaction #79861
title compound
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2cn([C@H]3CC[C@H](N4CCN(C)CC4)CC3)c3ncnc(N)c23)ccc1Oc1ccccc1
Reaction #79862
title compound
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(Br)ccc1Oc1ccccc1
Reaction #79863
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OB(c2ccc(Oc3ccccc3)c([N+](=O)[O-])c2)OC1(C)C
Reaction #79864
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc(Br)cc1Oc1ccccc1
Reaction #79866
title compound
Ausbeute 46.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OB(c2ccc(Oc3ccccc3)c(C=O)c2)OC1(C)C
Reaction #79867
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN([C@H]2CC[C@H](n3cc(-c4ccc(CC(=O)Nc5ccccc5)cc4)c4c(N)ncnc43)CC2)CC1.O=C(O)/C=C\C(=O)O.O=C(O)/C=C\C(=O)O.O=C(O)/C=C\C(=O)O
Reaction #79902
trans-N-phenyl-2-(4-{4-amino-7-[4-(4-methylpiperazino)cyclohexyl]-7H-pyrrolo[2,3-d]pyrimidin-5-yl}phenyl)acetamide trismaleate
DOI: 10.6084/m9.figshare.5104873.v1
Oc1cc(O)c2c(c1)O[C@H](c1cc(O)c(O)c(O)c1)[C@H](O)C2
Reaction #93587
(-) Epigallocatechin
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCOC(=O)c1cc(O)c(O)c(O)c1
Reaction #93589
n-octyl gallate
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
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