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233012

CCCCCCCCCCCCCCCCCCNC(=O)CCC(C)C1CCC2C3CCC4CC(OC(=O)ON5C(=O)CCC5=O)CCC4(C)C3CCC12C
Reaction #49208
Compound 89
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCCNC(=O)CCC(C)C1CCC2C3CCC4CC(OC(=O)NCCCCCC(=O)N5CC(O)CC5C(OC(c5ccc(OC)cc5)c5ccc(OC)cc5)c5ccccc5)CCC4(C)C3CCC12C
Reaction #49209
Compound 90
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2ncc(=O)n(CCC3CCC(=O)CC3)c2c1
Reaction #68024
7-methoxy-1-(2-(4-oxocyclohexyl)ethyl)quinoxalin-2(1H)-one
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
O=C([O-])[O-]
Reaction #83122
carbonate
Ausbeute 20.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cccc1CCNC(=O)C(C)(Cc1c[nH]c2ccccc12)NC(=O)OC1C2CC3CC(C2)CC1C3
Reaction #83132
Tricyclo[3.3.1.13,7 ]dec-2-yl (±)-[1-(1H-indol-3-ylmethyl)-1-methyl-2-[[2-(1-methyl-1H-pyrrol-2-yl) ethyl]amino]-2-oxoethyl]carbamate
DOI: 10.6084/m9.figshare.5104873.v1
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