Teilstruktursuche

1247860

CC(=O)NCCO/N=C/c1cc(C(=O)NOCCO)c(Nc2ccc(I)cc2F)c(F)c1F
Reaction #49029
(E)-5-[(2-Acetylamino-ethoxyimino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NCCONCc1cc(C(=O)NOCCO)c(Nc2ccc(I)cc2F)c(F)c1F
Reaction #49030
5-[(2-acetylamino-ethoxyamino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide
Ausbeute 76.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(OCCON=C(C)c2ccc(C(C)(C)C)cc2)cc1O
Reaction #57924
4-{2-[1-(4-tert-butyl-phenyl)-ethylideneaminooxy]-ethoxy}-2-hydroxy-benzoic acid methyl ester
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1
C/C(=N\OCCOc1ccc(C(=O)O)c(O)c1)c1ccc(C(C)(C)C)cc1
Reaction #57925
title compound
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc(C=NOCCOc2ccc(C(=O)O)c(OCc3ccc(C(F)(F)F)cc3)c2)cc1
Reaction #57932
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(C(=NOCC(=O)O)C(=O)NC2C(=O)N3C(C(=O)O)=C(C=C(F)F)CS(=O)[C@H]23)cs1
Reaction #93027
7-[2-carboxymethoxyimino-2-(2-aminothiazol-4-yl)acetamido]-3-(2,2-difluorovinyl)-3-cephem-4-carboxylic acid-1-oxide
Ausbeute 27.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CC(c2csc(C3CCN(C(=O)Cn4nc(C(F)F)cc4C(F)F)CC3)n2)=NO1
Reaction #157983
3-[2-(1-{[3,5-Bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazole-5-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC1CCCCC1Cl)C1CC(c2csc(C3CCN(C(=O)Cn4nc(C(F)F)cc4C(F)F)CC3)n2)=NO1
Reaction #157984
2-Chlorocyclohexyl 3-[2-(1-{[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazole-5-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cn2ncc3c(Nc4ccc(I)cc4F)c(C(=O)NOC(C)(C)CO)cnc32)cc1
Reaction #166238
title compound
Ausbeute 49.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(CO)ONC(=O)c1cnc2[nH]ncc2c1Nc1ccc(I)cc1F
Reaction #166239
title compound
Ausbeute 11.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(CBr)CC(c2cnc3c(cnn3CC)c2NC2CCCCC2)=NO1
Reaction #174863
DOI: 10.1039/C8SC04228D
CCOC(=O)C(=NOC(C)(C)C(=O)OC(C)(C)C)c1csc(NC(c2ccccc2)(c2ccccc2)c2ccccc2)n1
Reaction #190569
DOI: 10.1039/C8SC04228D
CC(=NOCCOc1ccc(CC2SC(=O)NC2=O)cc1)c1ccccc1
Reaction #198635
DOI: 10.1039/C8SC04228D
CC(=NOCCOc1ccc(CC2SC(=O)NC2=O)cc1)c1ccc(O)cc1
Reaction #200589
DOI: 10.1039/C8SC04228D
C[C@H](O/N=C(\C(=O)NC1C(=O)N2C(C(=O)[O-])=C(CSc3nc4cn(C)ccc-4[n+]3C)CS[C@H]12)c1csc(N)n1)C(=O)O
Reaction #216065
title compound
Ausbeute 52.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccccc1C(=O)N1CC(O)CO1
Reaction #218732
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(C(COC(=O)OCCCC(CO[N+](=O)[O-])O[N+](=O)[O-])=C(C(=O)O)c2ccccc2)cc1
Reaction #225640
DOI: 10.1039/C8SC04228D
O=C(CO)N1CCN(c2ccc(C3=NOC(COc4ccon4)C3)cc2F)CC1
Reaction #227589
DOI: 10.1039/C8SC04228D
CC(=O)OCC(=C(C(=O)OCCCCC(CO[N+](=O)[O-])O[N+](=O)[O-])c1ccccc1)c1ccc(S(C)(=O)=O)cc1
Reaction #228042
DOI: 10.1039/C8SC04228D
CC(=O)OCC(=C(C(=O)OCCC(CO[N+](=O)[O-])O[N+](=O)[O-])c1ccccc1)c1ccc(S(C)(=O)=O)cc1
Reaction #231283
DOI: 10.1039/C8SC04228D
Seite 1Weiter