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Nc1ccc(F)c(F)c1F

CC(C)N(CCN)C(C)C.Cl.Cl
Reaction #4299
N,N-bis(1-Methylethyl)-1,2-ethanediamine, dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(/C(=N/OC2CCNC2=O)C(=O)N[C@@H]2C(=O)N3C(C(=O)[O-])=C(C[n+]4ccccc4)CS[C@H]23)cs1
Reaction #4867
7β-{(Z)-2-(2-aminothiazol-4-yl)-2-[(2-pyrrolidon-3-yl)oxyimino]acetamido}-3-(1-pyridiniomethyl)-3-cephem-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(/C(=N/OC2CCNC2=O)C(=O)N[C@@H]2C(=O)N3C(C(=O)[O-])=C(C[n+]4ccccc4)CS[C@H]23)cs1
Reaction #4868
7β-{(Z)-2-(2-aminothiazol-4-yl)-2-[(2-pyrrolidon-3-yl)oxyimino]acetamido}-3-(1-pyridiniomethyl)-3-cephem-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(/C(=N/OC2CCNC2=O)C(=O)N[C@@H]2C(=O)N3C(C(=O)[O-])=C(C[n+]4ccccc4)CS[C@H]23)cs1
Reaction #4869
7β-{(Z)-2-(2-aminothiazol-4-yl)-2-[(2-pyrrolidon-3-yl)oxyimino]acetamido}-3-(1-pyridiniomethyl)-3-cephem-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](C)Nc1ccc(F)c(F)c1F
Reaction #8524
title compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](C)Nc1ccc(F)c(F)c1F
Reaction #8525
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)Nc1ccc(F)c(F)c1F
Reaction #8526
title compound
Ausbeute 97.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)Nc1ccc(F)c(F)c1F
Reaction #8527
title compound
Ausbeute 95.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)Nc1ccc(F)c(F)c1F
Reaction #8528
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)Nc1ccc(F)c(F)c1F
Reaction #8529
title compound
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)Nc1ccc(F)c(F)c1F
Reaction #8530
title compound
Ausbeute 81.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)Nc1ccc(F)c(F)c1F
Reaction #8531
title compound
Ausbeute 97.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C)Nc1ccc(F)c(F)c1F
Reaction #8532
title compound
Ausbeute 95.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)Nc1ccc(F)c(F)c1F
Reaction #8533
title compound
Ausbeute 94.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(Nc1ccc(F)c(F)c1F)C(=O)O
Reaction #8534
title compound
Ausbeute 98.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(Nc1ccc(F)c(F)c1F)C(=O)O
Reaction #8535
title compound
Ausbeute 97.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(Nc1ccc(F)c(F)c1F)C(=O)O
Reaction #8536
title compound
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(Nc1ccc(F)c(F)c1F)C(=O)O
Reaction #8537
title compound
Ausbeute 91.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(Nc1ccc(F)c(F)c1F)C(=O)O
Reaction #8538
title compound
Ausbeute 99.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(Nc1ccc(F)c(F)c1F)C(=O)O
Reaction #8539
title compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
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