Recherche de Sous-structure

27602

O=C(NCCCSc1ccncc1)c1cc(Br)c(Br)s1
Reaction #6219
desired compound
Rendement 71.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N(C)[C@@H]1CC[C@H](NC(=O)OCc2ccccc2)[C@H](CS(=O)(=O)c2ccc(Br)cc2)C1
Reaction #7774
[(1S,2R,4R)-2-(4-Bromo-benzenesulfonylmethyl)-4-(isopropyl-methyl-amino)-cyclohexyl]-carbamic acid benzyl ester
Rendement 94.4%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
CON=C(C(=O)CBr)C(=O)NC1C(=O)N2C(C(=O)OCC(Cl)(Cl)Cl)=CC(C)S[C@H]12
Reaction #56558
2,2,2-trichloroethyl 2-methyl-7-(2-methoxyimino-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)c3csc(N)n3)[C@H]2S1
Reaction #56572
2,2,2-trichloroethyl 2-methyl-7-[2-hydroxyimino-2-(2-aminothiazol-4-yl)acetamido]-3-cephem-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CON=C(C(=O)NC1C(=O)N2C(C(=O)OCC(Cl)(Cl)Cl)=CC(C)S[C@H]12)c1csc(N)n1
Reaction #56573
2,2,2-trichloroethyl 2-methyl-7-[2-methoxyimino-2-(2-aminothiazol-4-yl)acetamido]-3-cephem-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)[C@H](C(=O)O)N2C(=O)C(Br)(Br)[C@H]2S1(=O)=O
Reaction #62971
6,6-dibromopenicillanic acid 1,1-dioxide
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(Sc2c[nH]c3ccc(C#N)cc23)CC1
Reaction #65168
3-[(1-methylpiperidin-4-yl)thio]-1H-indole-5-carbonitrile
Rendement 5.1%DOI: 10.6084/m9.figshare.5104873.v1
C=COC(=O)N1CCC(Sc2c[nH]c3ccc(Br)cc23)CC1
Reaction #65170
Vinyl 4-[(5-bromo-1H-indol-3-yl)thio]piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCCCn1cc(SC2CCN(C)CC2)c2cc(Br)ccc21
Reaction #65175
5-bromo-1-butyl-3-[(1-methylpiperidin-4-yl)thio]1H-indole
DOI: 10.6084/m9.figshare.5104873.v1
Brc1cccc(-c2nn3c(c2-c2ccncc2)SCCC3)c1
Reaction #66345
2-(3-bromo-phenyl)-3-pyridin-4-yl-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]thiazine
Rendement 50.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #84805
Example 19
Rendement 37.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(=C(O)CBr)N1C(=O)C(N2C(=O)c3ccccc3C2=O)C1S
Reaction #96117
methyl α-[4-mercapto-3-phthalimido-2-oxoazetidin-1-yl]-α-(2-bromo-1-hydroxyethylidene)-acetate
Rendement 72.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1ccccc1)NC1C(=O)N(C(C(=O)OCC(Cl)(Cl)Cl)=C(O)CBr)C1SC(=O)OCC1CC1
Reaction #96119
2,2,2-trichloroethyl α-[4-cyclopropylmethoxycarbonylthio-3-phenoxyacetamido-2-oxoazetidin-1-yl]-α-(2-bromo-1-hydroxyethylidene)-acetate
Rendement 83.5%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
O=C(O)C1=C(CBr)CS(=O)[C@@H]2C(NC(=O)c3ccccc3)C(=O)N12
Reaction #96233
7-benzamido-3-bromomethyl-3-cephem-4-carboxylic acid-1-oxide
Rendement 104.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C1=C(CBr)CS(=O)[C@@H]2C(NC=O)C(=O)N12
Reaction #96235
t-butyl 3-bromomethyl-7-formamido-3-cephem-4-carboxylate-1-oxide
Rendement 28.5%DOI: 10.6084/m9.figshare.5104873.v1
O=CNC1C(=O)N2C(C(=O)O)=C(CBr)CS(=O)[C@H]12
Reaction #96236
3-bromomethyl-7-formamido-3-cephem-4-carboxylic acid-1-oxide
Rendement 99.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccccc1)NC1C(=O)N2C(C(=O)O)=C(CBr)CS(=O)[C@H]12
Reaction #96240
3-bromomethyl-7-phenylacetamido-3-cephem-4-carboxylic acid-1-oxide
Rendement 102.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1ccccc1)NC1C(=O)N2C(C(=O)O)=C(CBr)C(Br)S(=O)[C@H]12
Reaction #96241
2-bromo-3-bromomethyl-7-phenoxyacetamido-3-cephem-4-carboxylic acid-1-oxide
Rendement 101.5%DOI: 10.6084/m9.figshare.5104873.v1
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