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1197651

COc1cccc2c1C(O)N(C(C)(C)c1ccccc1)C2=O
Reaction #49353
4-methoxy-3-hydroxy-2-(1-methyl-1-phenylethyl)isoindolinone
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1
COCOc1c(OC)ccc2c1C(O)N(C(C)(C)c1ccccc1)C2=O
Reaction #49547
4-methoxymethoxy-5-methoxy-3-hydroxy-2-(1-methyl-1-phenylethyl)isoindolinone
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1
COCOc1c(OC)cc(I)c2c1C(O)N(C(C)(C)c1ccccc1)C2=O
Reaction #49548
4-methoxymethoxy-5-methoxy-3-hydroxy-7-iodo-2-(1-methyl-1-phenyl ethyl)isoindolinone
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
COCOc1c(C)ccc2c1C(O)N(C(C)(C)c1ccccc1)C2=O
Reaction #49553
4-methoxymethoxy-5-methyl-3-hydroxy-2-(1-methyl-1-phenylethyl)isoindolinone
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
COCOc1c(C)cc(I)c2c1C(O)N(C(C)(C)c1ccccc1)C2=O
Reaction #49554
4-methoxymethoxy-5-methyl-3-hydroxy-7-iodo-2-(1-methyl-1-phenylethyl)isoindolinone
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OC1c2ccccc2C(=O)N1c1ccc2ccc(Cl)nc2n1)N1CCN(C(=O)C2CCCCC2)CC1
Reaction #55357
2-(7-Chloro-1,8-naphthyridin-2-yl)-3-(4-cyclohexylcarbonylpiperazin-1-yl)carbonyloxy-isoindolin-1-one
Ausbeute 69.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)NC(=O)c2ccccc2C(=O)OCC2=C(C(=O)[O-])N3C(=O)[C@@H](NC(=O)Cc4cccs4)[C@H]3SC2)cc1.[Na+]
Reaction #56294
7β-(2-thienylacetamido)-3-[2-(N-tosylcarbamoyl) benzoyloxy]methyl-3-cephem-4-carboxylic acid sodium salt
Ausbeute 58.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)NC(=O)c2ccccc2C(=O)OCC2=C(C(=O)O)N3C(=O)[C@@H](NC(=O)OC(C)(C)C)[C@H]3SC2)cc1
Reaction #56300
7β-(t-butoxycarbonyl)amino-3-[2-(N-tosylcarbamoyl)benzoyloxy]methyl-3-cephem-4-carboxylic acid
Ausbeute 42.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)NC(=O)c2ccccc2C(=O)OCC2=C(C(=O)O)N3C(=O)[C@@H](N)[C@H]3SC2)cc1
Reaction #56301
7β-amino-3-[2-(N-tosylcarbamoyl)benzoyloxy]methyl-3-cephem4-carboxylic acid
Ausbeute 90.4%DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(NCCNc2ncc(N3C(=O)c4ccccc4C3=O)c(-c3ccc(Cl)cc3Cl)n2)ccc1[N+](=O)[O-]
Reaction #60044
2-[2-({2-[(6-amino-5-nitro(2-pyridyl))amino]ethyl}amino)-4-(2,4-dichlorophenyl)pyrimidin-5-yl ]isoindoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(NCCNc2ncc(N3C(=O)c4ccccc4C3=O)c(-c3ccc(Cl)cc3Cl)n2)ccc1[N+](=O)[O-]
Reaction #60050
2-[2-({2-[(6-amino-5-nitro(2-pyridyl))amino]ethyl}amino)-4-(2,4-dichlorophenyl)pyrimidin-5-yl]isoindoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(NCCNc2ncc(N3C(=O)c4ccccc4C3=O)c(-c3ccc(Cl)cc3Cl)n2)ccc1[N+](=O)[O-]
Reaction #60069
2-[2-({2-[(6-amino-5-nitro(2-pyridyl))amino]ethyl}amino)-4-(2,4-dichlorophenyl)pyrimidin-5-yl]isoindoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(NCCNc2ncc(N3C(=O)c4ccccc4C3=O)c(-c3ccc(Cl)cc3Cl)n2)ccc1[N+](=O)[O-]
Reaction #60074
2-[2-({2-[(6-amino-5-nitro(2-pyridyl))amino]ethyl}amino)-4-(2,4-dichlorophenyl)pyrimidin-5-yl]isoindoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(NCCNc2ncc(N3C(=O)c4ccccc4C3=O)c(-c3ccc(Cl)cc3Cl)n2)ccc1[N+](=O)[O-]
Reaction #60084
2-[2-({2-[(6-amino-5-nitro(2-pyridyl))amino]ethyl}amino)-4-(2,4-dichlorophenyl)pyrimidin-5-yl]isoindoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(NCCNc2ncc(N3C(=O)c4ccccc4C3=O)c(-c3ccc(Cl)cc3Cl)n2)ccc1[N+](=O)[O-]
Reaction #60093
2-[2-({2-[(6-amino-5-nitro(2-pyridyl))amino]ethyl}amino)-4-(2,4-dichlorophenyl)pyrimidin-5-yl]isoindoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(NCCNc2ncc(N3C(=O)c4ccccc4C3=O)c(-c3ccc(Cl)cc3Cl)n2)ccc1[N+](=O)[O-]
Reaction #60129
2-[2-({2-[(6-amino-5-nitro(2-pyridyl))amino]ethyl}amino)-4-(2,4-dichlorophenyl)pyrimidin-5-yl]isoindoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(NCCNc2ncc(N3C(=O)c4ccccc4C3=O)c(-c3ccc(Cl)cc3Cl)n2)ccc1[N+](=O)[O-]
Reaction #60220
2-[2-({2-[(6-amino-5-nitro(2-pyridyl))amino]ethyl}amino)-4-(2,4-dichlorophenyl)pyrimidin-5-yl]isoindoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(NCCNc2ncc(N3C(=O)c4ccccc4C3=O)c(-c3ccc(Cl)cc3Cl)n2)ccc1[N+](=O)[O-]
Reaction #60229
2-[2-({2-[(6-amino-5-nitro(2-pyridyl))amino]ethyl}amino)-4-(2,4-dichlorophenyl)pyrimidin-5-yl]isoindoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[Si](OCc1ccc(-n2nc(C(C)(C)C)cc2NC(=O)N[C@H]2CC[C@@H](Oc3ccc4nnc(N5CCCC[C@@H]5C)n4c3)c3ccccc32)cc1OCCOS(C)(=O)=O)(C(C)C)C(C)C
Reaction #88927
title compound
Ausbeute 97.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[Si](OCc1ccc(-n2nc(C(C)(C)C)cc2NC(=O)N[C@H]2CC[C@@H](Oc3ccc4nnc(N5CCCC[C@@H]5C)n4c3)c3ccccc32)cc1OCCN(C)C)(C(C)C)C(C)C
Reaction #88928
1-{5-tert-Butyl-2-[3-(2-dimethylamino-ethoxy)-4-triisopropylsilanyloxymethyl-phenyl]-2H-pyrazol-3-yl}-3-{(1S,4R)-4-[3-((S)-2-methyl-piperidin-1-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy]-1,2,3,4-tetrahydro-naphthalen-1-yl}-urea
DOI: 10.6084/m9.figshare.5104873.v1
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