Поиск подструктуры

515660

C[C@@H](O)[C@H]1C(=O)N2C(C(=O)O)=C(S[C@@H]3CN[C@H](C(O)c4csc5cncn45)C3)[C@H](C)[C@H]12
Reaction #655401
title compound
Выход 20.8%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)C1=C(S[C@H]2C[C@@H](C(O)c3csc4cn(C)c[n+]34)N(C(=O)OCC=C)C2)[C@H](C)[C@@H]2[C@@H]([C@@H](C)O)C(=O)N12.[I-]
Reaction #655402
allyl(1R,5S,6S)-6-((1R)-1-hydroxyethyl)-2-[(3S,5S)-1-allyloxycarbonyl-5-[1-hydroxy-1-(6-methylimidazo[5,1-b]thiazolium-3-yl)methyl]pyrrolidin-3-yl]thio-1-methylcarbapen-2-em-3-carboxylate iodide
Выход 95.2%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)C1=C(S[C@H]2C[C@@H](C(O)c3csc4cncn34)N(C(=O)OCC=C)C2)[C@H](C)[C@@H]2[C@@H]([C@@H](C)O)C(=O)N12
Reaction #655403
allyl(1R,5S,6S)-2-[(3S,5S)-1-allyloxycarbonyl-5-[1-hydroxy-1-(imidazo[5,1-b]thiazol-3-yl)methyl]pyrrolidin-3-yl]thio-6-((1R)-1-hydroxyethyl)-1-methylcarbapen-2-em-3-carboxylate
Выход 66.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)O)=C(S[C@@H]3CN[C@H](C(O)c4csc5cncn45)C3)[C@H](C)[C@H]12
Reaction #655404
colorless flocculent material
Выход 45.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)C1=C(S[C@H]2C[C@@H](C(O)c3csc4cn(C)c[n+]34)N(C(=O)OCC=C)C2)[C@H](C)[C@@H]2[C@@H]([C@@H](C)O)C(=O)N12.[I-]
Reaction #655405
allyl(1R,5S,6S)-2-[(3S,5S)-1-allyloxycarbonyl-5-[1-hydroxy-1-(6-methylimidazo[5,1-b]thiazolium-3-yl)methyl]pyrrolidin-3-yl]thio-6-((1R)-1-hydroxyethyl)-1-methylcarbapen-2-em-3-carboxylate iodide
Выход 97.4%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)O)=C(S[C@@H]3CN[C@H](C(O)c4csc5cn(C)c[n+]45)C3)[C@H](C)[C@H]12.[O-][Cl+3]([O-])([O-])[O-]
Reaction #655406
light orange flocculent material
Выход 68.4%DOI: 10.6084/m9.figshare.5104873.v1