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CCc1cc(CC)cc(CC)c1

CCOC(=O)c1cnc(Nc2cc(Cl)ccn2)o1
Reaction #449
Ausbeute 0.0%
CCOC(=O)c1cnc(Nc2cc(Cl)ccn2)o1
Reaction #451
Ausbeute 0.0%
Clc1ccnc(Nc2ncco2)c1
Reaction #454
Ausbeute 0.0%
C=CCN(C(=O)OCc1ccccc1)c1cnc2n(c1=O)[C@H](C(=O)Nc1ccccc1)C[C@@]2(C)N=[N+]=[N-]
Reaction #11065
azide
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cc(Cc2cc(C(C)C)c(N=Cc3ccccn3)c(C(C)C)c2)cc(C(C)C)c1N=Cc1ccccn1
Reaction #46066
18a
Ausbeute 70.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1nc(OS(=O)(=O)c2c(C(C)C)cc(C(C)C)cc2C(C)C)c2sc(=O)n([C@@H]3O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@H]3OC(C)=O)c2n1
Reaction #47752
5-acetylamino-7-(2,4,6-triisopropyl-benzenesulfonyloxy)-3-(2′,3′,5′-tri-O-acetyl-β-D-ribofuranosyl)thiazolo[4,5-d]pyrimidin-2-one
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCCCCCCCCC(=O)OCCOc1ccc(C2C(=O)Oc3c2cc(C(C)(C)C)cc3C(C)(C)C)cc1
Reaction #50778
5,7-di-tert-butyl-3-[4-(2-stearoyloxyethoxy)phenyl]benzofuran-2-one
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](c1ccccc1)[C@H](N=[N+]=[N-])C(=O)N1C(=O)OC[C@@H]1c1ccccc1
Reaction #61115
(S)-3-((2S,3R)-2-azido-3-phenyl-butyryl)-4-phenyl-oxazolidin-2-one
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(C(=O)c2cc3c(cc2O)CCC3)cc(C(C)(C)C)c1O
Reaction #65219
5-(3,5-di -tert-butyl-4-hydroxybenzoyl)-6-hydroxyindan
Ausbeute 83.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(Cc2cc(C(C)(C)C)cc(C(C)(C)C)c2)CCCCC1=O
Reaction #65912
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(C(c2ccc([N+](=O)[O-])cc2)N2CCCCC2)cc(C(C)(C)C)c1O
Reaction #81030
title compound
Ausbeute 23.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(C(c2cccc([N+](=O)[O-])c2)N2CCCCC2)cc(C(C)(C)C)c1O
Reaction #81031
title compound
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1cc(C(c2ccc(C#N)cc2)N2CCCCC2)cc(C(C)(C)C)c1O
Reaction #81032
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCc1cc(CCN)cc(Cc2ccc(F)cc2)c1
Reaction #81609
title compound
Ausbeute 62.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCc1cc(CCNS(=O)(=O)c2ccc(Cl)cc2)cc(Cc2ccc(F)cc2)c1
Reaction #81610
title compound
Ausbeute 73.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCc1cc(CCNS(=O)(=O)c2ccc(Cl)cc2)cc(Cc2ccc(F)cc2)c1
Reaction #81611
title compound
Ausbeute 82.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(=O)c2cc(CCNS(=O)(=O)c3ccc(Cl)cc3)cc(CCC(=O)O)c2)cc1
Reaction #81612
title compound
Ausbeute 85.9%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(C(=O)c2cc(CCNS(=O)(=O)c3ccc(Cl)cc3)cc(CCC(=O)O)c2)cc1
Reaction #81613
title compound
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCc1cc(CCNS(=O)(=O)c2ccc(Cl)cc2)cc(C(O)c2ccc(F)cc2)c1
Reaction #81614
title compound
Ausbeute 71.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCOc1ccc(NC(=O)Nc2ccccc2CCc2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)cc1
Reaction #82127
N-[2-(3,5-di-tert-butyl-4-hydroxyphenethyl)phenyl]-N'-(4-hexyloxyphenyl)urea
Ausbeute 71.1%DOI: 10.6084/m9.figshare.5104873.v1
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