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CC1(C)S[C@@H]2[C@H](NC(=O)CCC[C@H](N)C(=O)O)C(=O)N2[C@H]1C(=O)O
Reaction #1525
isopenicillin N
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)S[C@@H]2[C@H](NC(=O)CCC[C@H](N)C(=O)O)C(=O)N2[C@H]1C(=O)O
Reaction #2780
isopenicillin N
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC/C=C\C/C=C\C/C=C\CCCCC(=O)OCCCOC(=O)C1N2C(=O)C(NC(=O)COc3ccccc3)C2SC1(C)C
Reaction #56580
1-(3,3-dimethyl-7-oxo-6([phenoxyacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptan-2-oyloxy)-3-(z,z,z-octadeca-6,9,12-trienoyloxy)propane
DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)[C@@H](NC(=O)COc3ccccc3)[C@H]2SC1
Reaction #75330
(6R,7R) 3-Methyl-7-phenoxyacetamidoceph-3-em-4-carboxylic Acid Diphenylmethyl Ester
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)S[C@@H]2[C@H](N)C(=O)N2[C@H]1C(=O)O
Reaction #93272
6-aminopenicillanic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)S[C@@H]2[C@H](NC(=O)[C@H](N)c3ccccc3)C(=O)N2[C@H]1C(=O)[O-].[Na+]
Reaction #94330
sodium ampicillin
Ausbeute 98.7%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)S[C@@H]2[C@H](NC(=O)[C@H](N)c3ccccc3)C(=O)N2[C@H]1C(=O)[O-].[Na+]
Reaction #94331
sodium ampicillin
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)S[C@@H]2[C@H](NC(=O)[C@H](N)c3ccccc3)C(=O)N2[C@H]1C(=O)[O-].[Na+]
Reaction #94332
sodium ampicillin
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC(Cc1c[nH]c2ccccc12)C(=O)O
Reaction #174458
DOI: 10.1039/C8SC04228D
CC1(CSC#N)SC2C(NC(=O)Cc3ccccc3)C(=O)N2C1C(=O)OCC(Cl)(Cl)Cl
Reaction #197072
DOI: 10.1039/C8SC04228D
CC(=O)SCC1(C)SC2C(NC(=O)Cc3ccccc3)C(=O)N2C1C(=O)OCC(Cl)(Cl)Cl
Reaction #211314
DOI: 10.1039/C8SC04228D
CC1(C)C(C(=O)O)N2C(=O)C(NC(=O)COc3ccccc3)C2S1=O
Reaction #212016
DOI: 10.1039/C8SC04228D
COC(=O)C1N2C(=O)C(NC(=O)COc3ccccc3)C2SC1(C)CSc1nnc(C)s1
Reaction #213286
DOI: 10.1039/C8SC04228D
CC1(C)S[C@@H]2[C@H](N)C(=O)N2[C@H]1C(=O)O
Reaction #215179
6-amino-penicillanic acid
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)C1N2C(=O)[C@@H](NC(=O)C(C(=O)OC)=C3SCCS3)[C@H]2SC1(C)C
Reaction #215682
title compound
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(C(=O)N[C@@H]1C(=O)N2C(C(=O)[O-])C(C)(C)S[C@H]12)=C1SCCS1.[Na+]
Reaction #215683
title compound
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)C1N2C(=O)[C@@H](NC(=O)C(C(=O)OCC)=C3SCCS3)[C@H]2SC1(C)C
Reaction #215684
title compound
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C(=O)N[C@@H]1C(=O)N2C(C(=O)O)C(C)(C)S[C@H]12)=C1SCCS1
Reaction #215685
title compound
Ausbeute 73982.5%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)CC(=O)N[C@@H]1C(=O)N2C(C(=O)OCC=C)C(C)(C)S[C@H]12
Reaction #215686
title compound
Ausbeute 46.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)S[C@@H]2[C@H](NC(=O)C(C(=O)[O-])=C3SCCS3)C(=O)N2C1C(=O)[O-].[Na+].[Na+]
Reaction #215687
title compound
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
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