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O=C(COc1ccccc1)N[C@@H]1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=C(O)CS[C@H]12
Reaction #54392
7β-phenoxyacetamido-3-hydroxy-ceph-3-em-4-carboxylic acid p-nitrobenzyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1ccccc1)N[C@@H]1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=C(O)CS[C@H]12
Reaction #54393
7β-phenoxyacetamido-3-hydroxy-ceph-3-em-4-carboxylic acid p-nitrobenzyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1ccccc1)NC1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=C(O)CS[C@H]12
Reaction #96123
p-nitrobenzyl 3-hydroxy-7-phenoxyacetamido-3-cephem-4-carboxylate
収率 66.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1ccccc1)NC1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=C(O)CS[C@H]12
Reaction #96124
p-nitrobenzyl 3-hydroxy-7-phenoxyacetamido-3-cephem-4-carboxylate
収率 70.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1ccccc1)NC1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=C(O)CS[C@H]12
Reaction #96127
p-nitrobenzyl 3-hydroxy-7-phenoxyacetamido-3-cephem-4-carboxylate
収率 63.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccccc1)NC1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=C(O)CS[C@H]12
Reaction #96128
p-nitrobenzyl 7-phenylacetamido-3-hydroxy-3-cephem-4-carboxylate
収率 71.0%DOI: 10.6084/m9.figshare.5104873.v1
COC1=CS[C@@H]2[C@H](NC(=O)COc3ccccc3)C(=O)N2[C@H]1C(=O)O
Reaction #214635
7β-phenoxyacetamido-3-methoxy-ceph-2-em-4α-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1ccccc1)N[C@@H]1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=C(O)CS[C@H]12
Reaction #214653
7β-phenoxyacetamido-3-hydroxy-ceph-3-em-4-carboxylic acid p-nitrobenzyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1ccccc1)N[C@@H]1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=C(O)CS[C@H]12
Reaction #214654
7β-phenoxyacetamido-3-hydroxy-ceph-3-em-4-carboxylic acid p-nitrobenzyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1ccccc1)NC1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=C(O)CS[C@H]12
Reaction #412656
p-nitrobenzyl 3-hydroxy-7-phenoxyacetamido-3-cephem-4-carboxylate
収率 70.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1ccccc1)NC1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=C(O)CS[C@H]12
Reaction #412658
p-nitrobenzyl 3-hydroxy-7-phenoxyacetamido-3-cephem-4-carboxylate
収率 63.0%DOI: 10.6084/m9.figshare.5104873.v1
NC1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=C(O)CS[C@H]12
Reaction #451715
4-nitrobenzyl 7-amino-3-hydroxy-3-cephem-4-carboxylate
収率 69.5%DOI: 10.6084/m9.figshare.5104873.v1
CON=C(C(=O)NC1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=C(O)CS[C@H]12)c1csc(NC=O)n1
Reaction #451716
4-nitrobenzyl 7-[2-(2-formamido-4-thiazolyl)-2-methoxyiminoacetamido]-3-hydroxy-3-cephem-4-carboxylate
収率 43.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCON=C(C(=O)NC1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=C(O)CS[C@H]12)c1csc(NC=O)n1
Reaction #451739
4-nitrobenzyl 7-[2-(2-formamidothiazol-4-yl)-2-propoxyiminoacetamido]-3-hydroxy-3-cephem-4-carboxylate
収率 63.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CON=C(C(=O)NC1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=C(O)CS[C@H]12)c1csc(NC=O)n1
Reaction #451740
4-nitrobenzyl 7-[2-(2-formamidothiazol-4-yl)-2-isobutoxyiminoacetamido]-3-hydroxy-3-cephem-4-carboxylate
収率 90.6%DOI: 10.6084/m9.figshare.5104873.v1
CCON=C(C(=O)NC1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=C(O)CS[C@H]12)c1csc(NC=O)n1
Reaction #451741
4-nitrobenzyl 7-[2-(2-formamidothiazol-4-yl)-2-ethoxyiminoacetamido]-3-hydroxy-3-cephem-4-carboxylate
収率 77.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCON=C(C(=O)NC1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=C(OC)CS[C@H]12)c1csc(NC=O)n1
Reaction #451759
4-nitrobenzyl 7-[2-(2-formamidothiazol-4-yl)-2-butoxyiminoacetamido]-3-methoxy-3-cephem-4-carboxylate
収率 77.9%DOI: 10.6084/m9.figshare.5104873.v1
CCCCON=C(C(=O)NC1C(=O)N2C(C(=O)O)=C(OC)CS[C@H]12)c1csc(NC=O)n1
Reaction #451760
7-[2-(2-formamidothiazol-4-yl)-2-butoxyiminoacetamido]-3-methoxy-3-cephem-4-carboxylic acid
収率 75.3%DOI: 10.6084/m9.figshare.5104873.v1
CON=C(C(=O)NC1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)C(O)CS[C@H]12)c1csc(NC=O)n1
Reaction #451771
4-nitrobenzyl 7-[2-(2-formamido-4-thiazolyl)-2-methoxyiminoacetamido]-3-hydroxycepham-4-carboxylate
収率 76.7%DOI: 10.6084/m9.figshare.5104873.v1
CON=C(C(=O)NC1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=C(Cl)CS[C@H]12)c1csc(NC=O)n1
Reaction #451774
4-nitrobenzyl 7-[2-(2-formamido-4-thiazolyl)-2-methoxyiminoacetamido]-3-chloro-3-cephem-4-carboxylate
収率 19.4%DOI: 10.6084/m9.figshare.5104873.v1
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