Recherche de Sous-structure

725304

CC(=O)OCc1nc(C(Cl)Cl)cnc1N1C(=O)c2ccccc2C1=O
Reaction #4535
3-acetoxymethyl-5-dichloromethyl-2-phthalimidopyrazine
Rendement 77.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1c1ncc(C(Cl)Cl)nc1CO
Reaction #4536
5-dichloromethyl-3-hydroxymethyl-2-phthalimidopyrazine
Rendement 54.0%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1nc(C(Cl)Cl)cnc1N1C(=O)c2ccccc2C1=O
Reaction #4537
colorless crystals
Rendement 78.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1C1N=CC(C(Cl)Cl)=NC1=NO
Reaction #4538
colorless crystals
Rendement 67.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1c1ncc(C(Cl)Cl)nc1CO
Reaction #4540
5-dichloromethyl-3-hydroxymethyl-2-phthalimidopyrazine
Rendement 47.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1C=C(C(=O)OCC(Cl)(Cl)Cl)N2C(=O)C(NC(=O)CC(=O)CBr)[C@H]2S1
Reaction #56556
2,2,2-trichloroethyl 2-methyl-7-(3 -oxo-4-bromobutyramido)-3-cephem-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC1C=C(C(=O)OCC(Cl)(Cl)Cl)N2C(=O)C(NC(=O)C(=NO)C(=O)CBr)[C@H]2S1
Reaction #56557
2,2,2-trichloroethyl 2-methyl-7-(2-hydroxyimino-3-oxo-4-bromobutyramido)-3-cephem-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(C=C(Cl)Cl)CC(=O)N1CCOCC1
Reaction #62057
2
Rendement 72927.5%DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(Cl)oc(N2CCOCC2)c1
Reaction #62058
3
Rendement 75.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccccc1)NC1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=C(C=C(Cl)Cl)CS(=O)[C@H]12
Reaction #93025
benzhydryl 7-phenylacetamido-3-(2,2-dichlorovinyl)-3-cephem-4-carboxylate-1-oxide
Rendement 42.6%DOI: 10.6084/m9.figshare.5104873.v1
CON=C(C(=O)NC1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=C(C=C(Cl)Cl)CS[C@H]12)c1csc(NC=O)n1
Reaction #93029
benzhydryl 7-[2-methoxyimino-2-(2-formamidothiazol-4-yl)acetamido]-3-(2,2-dichlorovinyl)-3-cephem-4-carboxylate
Rendement 67.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(=C(C(=O)OCC(Cl)(Cl)Cl)N1C(=O)C2N=C(COc3ccccc3)SC21)N1CCOCC1
Reaction #96108
2,2,2-trichloroethyl α-[3-phenoxymethyl-7-oxo-4-thia-2,6-diazabicyclo[3,2,0]hept-2-en-6-yl]-α-(1-morpholinoethylidene)acetate
Rendement 50.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=C(C(=O)OCC(Cl)(Cl)Cl)N1C(=O)C2N=C(Cc3ccccc3)SC21)N1CCOCC1
Reaction #96110
2,2,2-trichloroethyl α-[3-benzyl-7-oxo-4-thia-2,6-diazabicyclo[3,2,0]hept-2-en-6-yl]-α-(1-morpholinoethylidene)acetate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1ccccc1)NC1C(=O)N2C(C(=O)OCC(Cl)(Cl)Cl)C(=O)CS[C@H]12
Reaction #96120
2,2,2-trichloroethyl 7-phenoxyacetamido-3-oxocepham-4-carboxylate
Rendement 124.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(cc1SC(Cl)(Cl)Cl)CCN(C(C)=O)CC2
Reaction #177637
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
Cc1onc(-c2ccccc2Cl)c1C(=O)NC1C(=O)N2C1SC(C)(CSc1nnnn1C)C2C(=O)OCC(Cl)(Cl)Cl
Reaction #187841
DOI: 10.1039/C8SC04228D
COc1cc(C(=O)N2CCCC2CO)c(NC(=O)OCC(Cl)(Cl)Cl)c(OC)c1C
Reaction #195031
DOI: 10.1039/C8SC04228D
CN1C(=O)C(C(=O)C(c2ccccc2)c2ccccc2)C(=O)N(C)C1=O
Reaction #200525
DOI: 10.1039/C8SC04228D
O=C1c2ccccc2C(=O)N1CCCOC(Cl)Cl
Reaction #205301
DOI: 10.1039/C8SC04228D
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