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539311

Cc1ccc(CCC(=O)N2C[C@H](C)N(Cc3ccc(F)cc3)C[C@H]2C)c(O)c1
Reaction #11705
title compound
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)COc1cc(C)ccc1CCC(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C
Reaction #11706
title compound
Ausbeute 103.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1[N+](=O)[O-]
Reaction #11728
title compound
Ausbeute 92.5%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1N
Reaction #11729
title compound
Ausbeute 69.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCc1cc(Cl)ccc1OCC(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C
Reaction #11753
title compound
Ausbeute 95.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1CCC(=O)O
Reaction #11754
title compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1CCC(=O)NS(C)(=O)=O
Reaction #11755
title compound
Ausbeute 46.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(OCC(=O)N2C[C@H](C)N(Cc3ccc(F)cc3)C[C@H]2C)c(CCC(=O)NS(C)(=O)=O)n1
Reaction #11792
title compound
Ausbeute 42.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Cc1cc(Cl)ccc1OCC(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C)[N+](=O)[O-]
Reaction #11793
title compound
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(N)Cc1cc(Cl)ccc1OCC(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C
Reaction #11794
title compound
Ausbeute 100.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(COc2cc(Cl)ccc2OCC(=O)N2C[C@H](C)N(Cc3ccc(F)cc3)C[C@H]2C)nc1
Reaction #11806
title compound
Ausbeute 86.6%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1OCc1ccc(C(=O)O)cn1
Reaction #11807
title compound
Ausbeute 27.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1C1CCC(=O)O1
Reaction #11811
title compound
Ausbeute 109.5%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ncc(Cl)cc1[N+](=O)[O-]
Reaction #11812
title compound
Ausbeute 89.4%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ncc(Cl)cc1N
Reaction #11813
title compound
Ausbeute 92.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1-c1ccno1
Reaction #11821
title compound
Ausbeute 101.5%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1C(=O)CC#N
Reaction #11822
title compound
Ausbeute 74.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1N[C@H]2C/C=C\C[C@@H]1N(c1ccc3ccccc3c1)C2=O
Reaction #68902
Z-(1S,6S)-7-naphthalen-2-yl-7,9-diaza-bicyclo[4.2.2]dec-3-ene-8,10-dione
DOI: 10.6084/m9.figshare.5104873.v1
C1=C\C[C@H]2CN[C@@H](C/1)CN2c1ccc2ccccc2c1
Reaction #68903
Z-(1S,6S)-7-naphthalen-2-yl-7,9-diaza-bicyclo[4.2.2]dec-3-ene
DOI: 10.6084/m9.figshare.5104873.v1
C1=CCC2CNC(C1)CN2c1ccc2c(c1)Cc1ccccc1-2
Reaction #68904
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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