Busqueda de Subestructura

CC(=C)CCl

O=C(O)C1=C(CCl)CS[C@@H]2[C@H](NC(=S)Cc3cc(Cl)ccc3Cl)C(=O)N12
Reaction #3761
(6R)-trans-3-chloromethyl-7-[(2,5-dichlorophenyl)-thioacetamido]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
Rendimiento 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(ON=C(C(=O)N[C@@H]1C(=O)N2C(C(=O)[O-])=C(C[N+](C)(C)Cc3cc(=O)c(O)c[nH]3)CS[C@H]12)c1nsc(N)n1)C(=O)O
Reaction #5613
7β-[2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(1-carboxy-1-methylethoxyimino)acetamido]-3-[N,N-dimethyl-N-{(5-hydroxy-4-oxo-1,4-dihydropyridin-2-yl)methyl}ammonio]methyl-3-cephem-4carboxylate
Rendimiento 29.2%DOI: 10.6084/m9.figshare.5104873.v1
C=CCON=C(C(=O)N[C@@H]1C(=O)N2C(C(=O)[O-])=C(C[N+]3(C)CCN(C(=O)c4cc(O)c(O)cn4)CC3)CS[C@H]12)c1nsc(N)n1
Reaction #5624
7β-[2-(5-amino-1,2,4-thiadiazol-3-yl)-2-allyloxyiminoacetamido]-3-[1-methyl-4-(4,5-dihydroxy-2-pyridylcarbonyl)-1-piperazinio]methyl-3-cephem-4-carboxylate
Rendimiento 34.2%DOI: 10.6084/m9.figshare.5104873.v1
C=C1Cn2c(=O)ccc3ncc(F)c1c32
Reaction #43397
solid
Rendimiento 36.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(CCl)c1c(F)cnc2cc(F)c(OC)nc12
Reaction #43413
8-[1-(Chloromethyl)ethenyl]-3,7-difluoro-2-(methyloxy)-1,5-naphthyridine
DOI: 10.6084/m9.figshare.5104873.v1
C=C1Cn2c(=O)c(F)cc3ncc(F)c1c32
Reaction #43414
3,8-Difluoro-4-methylidene-4,5-dihydro-7H-pyrrolo[3,2,1-de]-1,5-naphthyridin-7-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)N(NC(=O)C1=CCCCC1)C(=O)c1ccccc1
Reaction #49913
N'-t-butyl-N-cyclohexenylcarbonyl-N'-benzoylhydrazine
DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(C)C(Cl)N(c2ccc(Cl)c(Cl)c2)C1=O
Reaction #55465
N-(3',4'-Dichlorophenyl)-3,4-dimethyl-2-chloro-5-oxo-2,5-dihydropyrrole
DOI: 10.6084/m9.figshare.5104873.v1
C=C(CCl)[C@H](C(=O)OC(c1ccccc1)c1ccccc1)N1C(=O)[C@@H]2N=C(c3ccccc3)O[C@@H]21
Reaction #55517
Compound ( 7 )
DOI: 10.6084/m9.figshare.5104873.v1
C=C(CCl)[C@H](C(=O)OC(c1ccccc1)c1ccccc1)N1C(=O)[C@@H]2N=C(c3ccccc3)O[C@@H]21
Reaction #55518
Compound ( 7 )
DOI: 10.6084/m9.figshare.5104873.v1
C=C(CCl)[C@H](C(=O)OC(c1ccccc1)c1ccccc1)N1C(=O)[C@@H]2N=C(c3ccccc3)O[C@@H]21
Reaction #55519
Compound ( 7 )
DOI: 10.6084/m9.figshare.5104873.v1
CC(=Cc1ccc(C)cc1)CCl
Reaction #57396
title compound
Rendimiento 87.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(=Cc1ccc(C)cc1)COc1cc(C)c(NC=O)c(C)c1C
Reaction #57397
title compound
Rendimiento 78.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=C(CCl)CS[C@H]12)C(=NOC(F)F)c1csc(NC(c2ccccc2)(c2ccccc2)c2ccccc2)n1
Reaction #62773
benzhydryl 7-[2-(2-tritylaminothiazol-4-yl)- 2-difluoromethoxyiminoacetamido]-3-chloromethyl-3-cephem-4-carboxylate
Rendimiento 105.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=C(CCl)CS(=O)[C@H]12)C(=NOC(F)F)c1csc(NC(c2ccccc2)(c2ccccc2)c2ccccc2)n1
Reaction #62781
benzhydryl 7-[2-(2-tritylaminothiazol-4-yl)-2-difluoromethoxyiminoacetamido]-3-chloromethyl-3-cephem-4-carboxylate-1-oxide
Rendimiento 84.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=C(CI)CS(=O)[C@H]12)C(=NOC(F)F)c1csc(NC(c2ccccc2)(c2ccccc2)c2ccccc2)n1
Reaction #62782
benzhydryl 7-[2-(2-tritylaminothiazol-4-yl)-2-difluoromethoxyiminoacetamido]-3-iodomethyl-3-cephem-4-carboxylate-1-oxide
Rendimiento 42.4%DOI: 10.6084/m9.figshare.5104873.v1
N#CC(=Cc1ccccc1)C(=O)Cl
Reaction #64824
α-cyanocinnamoyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CC1=C2CCCC(C)(C)C2CCC1=O
Reaction #64852
tert.butyl 2-[5,5-dimethyl-2-oxo-2,3,4,4a,5,6,7,8-octahydronaphth-1-yl]acetate
Rendimiento 52.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1=C(CCl)CS[C@@H]2[C@H](NC(=S)Cc3cc(Cl)ccc3Cl)C(=O)N12
Reaction #81888
(6R)-trans-3-chloromethyl-7-[(2,5-dichlorophenyl)-thioacetamido]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
Rendimiento 72.8%DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(C)C(=O)C(CCl)=C(C)C1=O
Reaction #92084
2-chloromethyl-3,5,6-trimethyl-[1,4]benzoquinone
Rendimiento 81.0%DOI: 10.6084/m9.figshare.5104873.v1
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