部分構造検索

3158

O=C([O-])[C@H]1/C(=C/CO)O[C@@H]2CC(=O)N21.[K+]
Reaction #3722
potassium clavulanate
収率 73.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)[O-])=C(N=[N+]=[N-])C[C@H]12.[K+]
Reaction #416859
potassium (5R,6S)-2-azido-6-[(R)-1-hydroxyethyl]-carbapen-2-em-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])[C@H]1/C(=C/CO)O[C@@H]2CC(=O)N21.[K+]
Reaction #430038
potassium clavulanate
収率 70.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)[O-])=C(c3ncc4sccn34)[C@H](C)[C@H]12.[K+]
Reaction #469814
title compound
収率 32.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)[O-])=C(c3ncn4ccsc34)[C@H](C)[C@H]12.[K+]
Reaction #469821
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Nc2nccc(C(F)(F)F)n2)cc(-c2cnc([C@@]3(O)CC[C@H](C(=O)[O-])C(C)(C)C3)s2)c1.[K+]
Reaction #497739
potassium (1S,4R)-4-hydroxy-2,2-dimethyl-4-[5-(3-methyl-5-{[4-(trifluoromethyl)pyrimidin-2-yl]amino}phenyl)-1,3-thiazol-2-yl]cyclohexanecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(OC)c1-c1cc(C(=O)NC2(C(=O)[O-])C3CC4CC(C3)CC2C4)nn1-c1ccc(C(=O)N(C)CCCN(C)C)cc1C(C)C.[K+]
Reaction #669972
expected product
収率 56.8%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)([O-])c1cc(O)ccc1O.[K+]
Reaction #674992
2,5-dihydroxybenzenesulfonic acid potassium salt
収率 96.6%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)([O-])c1cc(O)ccc1O.[K+]
Reaction #674993
2,5-dihydroxybenzenesulfonic acid potassium salt
収率 77.9%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)([O-])c1cc(O)ccc1O.[K+]
Reaction #674994
2,5-dihydroxybenzenesulfonic acid potassium salt
収率 77.9%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)([O-])c1cc(O)ccc1O.[K+]
Reaction #674995
2,5-dihydroxybenzenesulfonic acid potassium salt
収率 87.6%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)[O-])=C(N=[N+]=[N-])C[C@H]12.[K+]
Reaction #934388
potassium (5R,6S)-2-azido-6-[(R)-1-hydroxyethyl]-carbapen-2-em-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CON=CC1=C(C(=O)[O-])N2C(=O)[C@@H](NC(=O)Cc3cccs3)[C@H]2SC1.O.[K+]
Reaction #1059671
potassium 3-methoxyiminomethyl-7β-(2-thienylacetamido)-3-cephem-4-carboxylate monohydrate
収率 181.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])[C@H]1/C(=C/CO)O[C@@H]2CC(=O)N21.[K+]
Reaction #1120553
potassium clavulanate
収率 70.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Nc2nccc(C(F)(F)F)n2)cc(-c2cnc([C@@]3(O)CC[C@H](C(=O)[O-])C(C)(C)C3)s2)c1.[K+]
Reaction #1127229
potassium (1S,4R)-4-hydroxy-2,2-dimethyl-4-[5-(3-methyl-5-{[4-(trifluoromethyl)pyrimidin-2-yl]amino}phenyl)-1,3-thiazol-2-yl]cyclohexanecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CON=CC1=C(C(=O)[O-])N2C(=O)[C@@H](NC(=O)Cc3cccs3)[C@H]2SC1.O.[K+]
Reaction #1375172
potassium 3-methoxyiminomethyl-7β-(2-thienylacetamido)-3-cephem-4-carboxylate monohydrate
収率 181.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC(CC)C(=O)[O-].[K+]
Reaction #1468169
potassium 2-ethylhexanoate salt
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=CC2(CC[C@H]1S(=O)(=O)[N-]c1ccc(F)cc1Cl)O[C@H](CO)[C@@H](CO)O2.[K+]
Reaction #1514246
crude product
収率 85.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=CC2(CC[C@H]1S(=O)(=O)[N-]c1ccc(F)cc1Br)O[C@H](CO)[C@@H](CO)O2.[K+]
Reaction #1514247
title compound
収率 65.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCCl)[C@H]1CC[C@H](C(=O)OCc2ccccc2)CC1
Reaction #1549177
desired product
収率 35.0%DOI: 10.6084/m9.figshare.5104873.v1
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