Teilstruktursuche

16528

CC(C)(C)OC(=O)n1cccc1-c1ccc2c(c1)C1(CCCCC1)C(=O)N2
Reaction #7095
subtitled compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1cccc1-c1ccc2c(c1)C1(CCCC1)C(=O)N2
Reaction #9411
2-(1′,2′-dihydro-2′-oxospiro[cyclopentane-1,3′-[3H]indol]-5′-yl)-1H-pyrrole-1-carboxylic acid, tert-butyl ester
Ausbeute 83.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1cccc1-c1ccc2c(c1)C1(CCCCC1)C(=O)N2
Reaction #9412
2-(1′,2′-dihydro-2′-oxospiro[cyclohexane-1,3′-[3H]indol]-5′-yl)-1H-pyrrole-1-carboxylic acid, tert-butyl ester
Ausbeute 77.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2cc3ccccc3n2C(=O)OC(C)(C)C)cc1C=O
Reaction #10742
2-(5-Formyl-2,4-dimethoxy-phenyl)-indole-1-carboxylic acid tert-butyl ester
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(OCOC)c(-c2cccn2C(=O)OC(C)(C)C)c1
Reaction #41538
compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1cccc1-c1cc([N+](=O)[O-])ccc1F
Reaction #41552
t-butyl 2-(2-fluoro-5-nitro-phenyl)-pyrrole-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1cccc1-c1cc([N+](=O)[O-])c(N)cc1Oc1ccc(S(C)(=O)=O)cc1
Reaction #41620
t-butyl 2-(4-amino-2-(4-methanesulfonyl-phenoxy)-5-nitro-phenyl)-pyrrole-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1cccc1-c1ccc(N)cc1F
Reaction #41631
compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Nc2cncc(-c3cccn3C(=O)OC(C)(C)C)n2)cc(OC)c1OC
Reaction #44534
pure title compound
Ausbeute 4.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2ccc(N)c3c2C(=O)NC3=O)cc2ccccc21
Reaction #49272
3-amino-6-[1-(tert-butoxycarbonyl)indol-2-yl]phthalimide
Ausbeute 67.7%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(S(=O)(=O)c2ccc3c(c2)cc(-c2cc(-c4ccccc4)c(N)c4c2C(=O)NC4=O)n3C(=O)OC(C)(C)C)CC1
Reaction #49276
3-amino-4-phenyl-6-[1-(tert-butoxycarbonyl)-5-(4-methylpiperazin-1-ylsulfonyl)indol-2-yl]phthalimide
Ausbeute 20.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2ccc(Cl)c3c2C(=O)NC3)cc2ccccc21
Reaction #49287
4-chloro-7-(1-(tert-butoxycarbonyl)indol-2-yl)isoindolinone
Ausbeute 44.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2ccc(Cl)c3c2C(=O)NC3)cc2cc(C#N)ccc21
Reaction #49398
4-chloro-7-[1-(tert-butoxycarbonyl)-5-cyanoindol-2-yl]isoindolinone
Ausbeute 42.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2cc3ccccc3n2C(=O)OC(C)(C)C)c2c(c1OS(C)(=O)=O)CNC2=O
Reaction #49565
4-methanesulfonyloxy-5-methoxy-7-(1-(tert-butoxycarbonyl)indol-2-yl)isoindolinone
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc(-c2c(OC)cccc2OC)cc1)NC(=O)c1c(Cl)cc(-c2cccn2C(=O)OC(C)(C)C)cc1Cl
Reaction #52965
N-[4-(1-tert-butoxycarbonyl-2-pyrrolyl)-2,6-dichlorobenzoyl]-4-(2,6-dimethoxyphenyl)-L-phenylalanine methyl ester
Ausbeute 92.1%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccccc1S(=O)(=O)Nc1ccc2[nH]nc(-c3cc4cccnc4[nH]3)c2c1
Reaction #53693
2-methylsulfonyl-N-[3-(1H-pyrrolo[2,3-b]pyridin-2-yl)-1H-indazol-5-yl]benzenesulfonamide
Ausbeute 45.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2[nH]c(-c3n[nH]c4ccc(NS(=O)(=O)c5ccccc5S(C)(=O)=O)cc34)cc2c1
Reaction #53694
2-methylsulfonyl-N-[3-(5-methoxy-1H-indol-2-yl)-1H-indazol-5-yl]benzenesulfonamide
Ausbeute 19.3%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccccc1S(=O)(=O)Nc1ccc2[nH]nc(-c3ccc[nH]3)c2c1
Reaction #53695
2-methylsulfonyl-N-[3-(1H-pyrrol-2-yl)-1H-indazol-5-yl]benzenesulfonamide
Ausbeute 29.9%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccccc1S(=O)(=O)Nc1ccc2[nH]nc(-c3cc4ccccc4[nH]3)c2c1
Reaction #53696
N-[3-(1H-indol-2-yl)-1H-indazol-5-yl]-2-methylsulfonylbenzenesulfonamide
Ausbeute 40.8%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1ccc2[nH]nc(-c3cc4ccccc4[nH]3)c2c1)c1ccccc1
Reaction #53715
N-[3-(1H-indol-2-yl)-1H-indazol-5-yl]benzenesulfonamide
Ausbeute 66.3%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter