部分構造検索

CCOCC=C(C)C

C=CC1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)COc3ccccc3)[C@H]2SC1
Reaction #5641
title compound
収率 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
収率 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
C=C(OCC)C1=C2c3ccc(OC)c(Cl)c3CC2(CCCC)CCC1=O
Reaction #7978
9a-butyl-8-chloro-4-(1-ethoxyvinyl)-7-methoxy-1,2,9,9a-tetrahydro-3H-fluoren-3-one
収率 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCC12CCC(=O)C(C(C)=O)=C1c1ccc(OC)c(Cl)c1C2
Reaction #7979
4-acetyl-9a-butyl-8-chloro-7-methoxy-1,2,9,9a-tetrahydro-3H-fluoren-3-one
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
収率 59.0%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 #65627
title compound
収率 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
収率 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
CC1CC(c2ccc(Cl)c(Cl)c2)=C(CO)CN1C(=O)OC(C)(C)C
Reaction #181598
DOI: 10.1039/C8SC04228D
CON=C(C(=O)NC1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=C(C=COS(=O)(=O)c3ccc(C)cc3)CSC12)c1csc(N)n1
Reaction #182673
DOI: 10.1039/C8SC04228D
C[NH-]
Reaction #183557
DOI: 10.1039/C8SC04228D
CC(C)CC1C(C=C(CCCOC2CCCCO2)C(=O)O)OC(C)(C)N1C(=O)OCc1ccccc1
Reaction #194051
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
CC(=CC1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(N)C2S(=O)C1)Sc1nnc(C)s1
Reaction #205403
DOI: 10.1039/C8SC04228D
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