子结构搜索

CC(C)=CCO

CCOC(=O)C1=C2COC=CN2C(C)=C(C(=O)OC)C1c1ccccc1Cl
Reaction #1349
title compound
收率 65.8%DOI: 10.6084/m9.figshare.5104873.v1
C[N+]1(CC2=C(C(=O)[O-])N3C(=O)[C@@H](NC(=O)C(=NOCC(=O)O)c4nsc(N)n4)[C@H]3SC2)CCNCC1
Reaction #5620
7β-[2-(5-amino-1,2,4-thiadiazol-3-yl)-2-carboxymethoxyiminoacetamido]-3-(1-methyl-1-piperazinio)methyl-3-cephem-4-carboxylate
收率 33.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)COc3ccccc3)[C@H]2SC1
Reaction #5641
title compound
收率 88.8%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C\C1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)COc3ccccc3)[C@H]2SC1
Reaction #5642
title compound
收率 92.9%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C\C1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)COc3ccccc3)[C@H]2SC1
Reaction #5644
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cn1nnnc1C=CC1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)COc3ccccc3)[C@H]2S(=O)C1
Reaction #54319
benzhydryl 7-phenoxyacetamido-3-(1-methyl-1H-tetrazol-5-yl)vinyl-3-cephem-4-carboxylate-1-oxide
收率 59.0%DOI: 10.6084/m9.figshare.5104873.v1
CNCc1ccccc1CC(=O)NC1C(=O)N2C(C(=O)O)=C(CSc3ccc4nn(CC(=O)O)c(=O)n4n3)CS[C@H]12
Reaction #55277
7-[o-(Methylaminomethyl)phenylacetamido]-3-(2-carboxymethyl-2,3-dihydro-s-triazolo[4,3-b]pyridazin-3-on-6-ylthiomethyl)-3-cephem-4-carboxylic Acid
DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)N(C)Cc1ccccc1CC(=O)NC1C(=O)N2C(C(=O)O)=C(CSc3ccc4nn(CCC(=O)O)c(=O)n4n3)CS[C@H]12
Reaction #55280
title compound
收率 50.0%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@]1(NC(=O)[C@H](O)c2ccccc2)C(=O)N2C(C(=O)O)=C(C(CCC(=O)O)Sc3nnn[nH]3)CS[C@@H]21
Reaction #55420
7β-D-Mandelamido-7α-methoxy-3-[1-(2-carboxyethyl)tetrazol-5-ylthiomethyl]-3-cephem-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
C=CC1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)COc3ccccc3)[C@H]2SC1
Reaction #65627
title compound
收率 88.8%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C\C1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)COc3ccccc3)[C@H]2SC1
Reaction #65628
title compound
收率 92.9%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C\C1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)COc3ccccc3)[C@H]2SC1
Reaction #65630
title compound
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
OCC(=C(c1ccc(F)cc1)c1ccc(F)cc1)c1nnn(C(c2ccccc2)(c2ccccc2)c2ccccc2)n1
Reaction #173372
DOI: 10.1039/C8SC04228D
CON=C(C(=O)NC1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=C(C=C(C)Sc3nnc(C)s3)CS(=O)C12)c1csc(NC(c2ccccc2)(c2ccccc2)c2ccccc2)n1
Reaction #173397
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=C(C=CCl)CS(=O)C12
Reaction #178654
DOI: 10.1039/C8SC04228D
C[NH-]
Reaction #183557
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(=CCO)C(C)(C)C1
Reaction #190031
DOI: 10.1039/C8SC04228D
CCOC(=O)C=C(C(=O)OCC)c1ccc2nc(C)ccc2c1
Reaction #198603
DOI: 10.1039/C8SC04228D
CCOC(=O)C1=C(COCc2nnn(CCN3CCN(C(=O)NC)CC3)n2)NC(C)=C(C(=O)OC)C1c1cccc(Cl)c1Cl
Reaction #202459
DOI: 10.1039/C8SC04228D
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