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829013

COC(=O)c1cccc(N2CCC(NC(=O)OC(C)(C)C)CC2)c1
Reaction #255
Ausbeute 13.8%
COC(=O)c1cc(C(=O)OC)cc(N2CCOCC2)c1
Reaction #492
Ausbeute 78.2%
CCCCN1CCNc2ccc(C(=O)OC)cc21
Reaction #42478
title compound
Ausbeute 45.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN1CCN(S(C)(=O)=O)c2ccc(C(=O)OC)cc21
Reaction #42479
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCN1CCOc2ccc(C(=O)OC)cc21
Reaction #42496
title compound
Ausbeute 80.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN1CCOc2ccc(C(=O)O)cc21
Reaction #42497
title compound
Ausbeute 98.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN1CCOc2ccc(C(=O)N[C@@H](Cc3cc(F)cc(F)c3)[C@H](O)CNCc3cccc(CC)c3)cc21
Reaction #42498
title compound
Ausbeute 17.9%DOI: 10.6084/m9.figshare.5104873.v1
CCN1C(=O)CC(C)(C)c2ccc(C#N)cc21
Reaction #64677
4,4-dimethyl-1-ethyl-1,2,3,4-tetrahydro-2-oxo-7-quinolinecarbonitrile
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1c(I)c(C(=O)OC(C)OC(=O)Oc2ccccc2)c(I)c(N(C)C(C)=O)c1I
Reaction #65063
1-(Phenyloxycarbonyloxy)ethyl 5-(N-acetylamino)-3-(N-acetyl-N-methylamino)-2,4,6-triiodobenzenecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(OC(=O)Oc1ccccc1)OC(=O)c1c(I)c(NC(C)=O)c(I)c(N(C)C(C)=O)c1I
Reaction #65069
1-(Phenyloxycarbonyloxy)pentyl 5-(N-acetylamino)-3-(N-acetyl-N-methylamino)-2,4,6-triiodobenzenecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1c(I)c(C(=O)OC(OC(=O)Oc2ccccc2)c2ccccc2)c(I)c(N(C)C(C)=O)c1I
Reaction #65070
1-(Phenyloxycarbonyloxy)-1-phenylmethyl 5-(N-acetylamino)-3-(N-acetyl-N-methylamino)-2,4,6-triiodobenzenecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1CN(c2cccc(C(=O)OC(C)(C)C)c2)CC[C@@H]1N
Reaction #71763
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(c3cccc(C(=O)OC(C)(C)C)c3)C[C@H]2OC)nc1C(F)(F)F
Reaction #71764
title compound
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(c3cccc(C(=O)O)c3)C[C@H]2OC)nc1C(F)(F)F
Reaction #71765
title compound
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@@H]1CN(c2cccc(C(=O)OC(C)(C)C)c2)CC[C@@H]1N
Reaction #71774
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@@H]1CN(c2cccc(C(=O)OC(C)(C)C)c2)CC[C@@H]1NC(=O)c1nc(C(F)(F)F)c(CC)[nH]1
Reaction #71775
title compound
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@@H]1CN(c2cccc(C(=O)O)c2)CC[C@@H]1NC(=O)c1nc(C(F)(F)F)c(CC)[nH]1
Reaction #71776
title compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(c3ccc(C)c(C(=O)OC)c3)C[C@H]2OC)nc1Cl
Reaction #72053
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(F)cc(N2CC[C@H](N)[C@H](OC)C2)c1
Reaction #72059
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(c3cc(F)cc(C(=O)OC)c3)C[C@H]2OC)nc1Cl
Reaction #72060
title compound
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1
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