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Sc1ccccc1

CCCCCCCCCCCCC1(Cc2cc(N=Nc3ccc([N+](=O)[O-])cc3S(C)(=O)=O)ccc2O)COCCOCC(C)(C)COCCOC1
Reaction #5635
Compound 16
Ausbeute 4.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(=O)NS(=O)(=O)c2ccccc2C#CCCCO)ccc1Cc1cn(C)c2ccc(NC(=O)OC3CCCC3)cc12
Reaction #6479
title compound
Ausbeute 97.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(=O)NS(=O)(=O)c2ccccc2C#CC(C)(C)OC(C)=O)ccc1Cc1cn(C)c2ccc(NC(=O)OC3CCCC3)cc12
Reaction #6480
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Cc1ccc2ccccc2c1)N1CCN(S(=O)(=O)c2ccccc2[N+](=O)[O-])C(CCCNC(=O)OCc2ccccc2)C1=O
Reaction #8624
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccccc1S(=O)(=O)Nc1ccc2[nH]nc(-c3ccco3)c2c1
Reaction #53691
N-(3-furan-2-yl-1 H-indazol-5-yl)-2-methylsulfonylbenzenesulfonamide
Ausbeute 32.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn(-c2cc([N+](=O)[O-])ccc2C(F)(F)F)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1F
Reaction #64580
title compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1ccccc1)n1ncc2c(-c3nnc(CN4CCOC5(CCCC5)C4)o3)cc(Br)cc21
Reaction #67121
title compound
Ausbeute 30.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2cc(-c3nnc(CN4CCCOCC4)o3)c3cnn(S(=O)(=O)c4ccccc4)c3c2)cc1NS(C)(=O)=O
Reaction #67124
N-(2-(Methyloxy)-5-{1-(phenylsulfonyl)-4-[5-(tetrahydro-1,4-oxazepin-4(5H)-ylmethyl)-1,3,4-oxadiazol-2-yl]-1H-indazol-6-yl}-3-pyridinyl)methanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2cc(-c3nnc(CN4CCOC5(CCCC5)C4)o3)c3cn[nH]c3c2)cc1NS(C)(=O)=O
Reaction #67157
title compound
Ausbeute 99.6%DOI: 10.6084/m9.figshare.5104873.v1
c1cc(-c2cc(-c3nnc(CN4CCOC5(CCCC5)C4)o3)c3cn[nH]c3c2)c2cc[nH]c2c1
Reaction #67162
title compound
Ausbeute 25.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(-c2cc(-c3nnc(CN4CCCOCC4)o3)c3cn[nH]c3c2)cc1NS(C)(=O)=O
Reaction #67165
title compound
Ausbeute 89.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(OCCCONC(=N)N)cc(OS(=O)(=O)c2ccccc2S(=O)(=O)N(CCC(=O)O)Cc2ccccc2)c1
Reaction #78009
title compound
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(OCCCONC(=N)N)cc(OS(=O)(=O)c2ccccc2S(=O)(=O)N(CCC#N)Cc2ccco2)c1
Reaction #78010
title compound
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=C1CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)C3=CC[C@]12C)C(Cl)S(=O)c1ccccc1
Reaction #94827
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=CCl)[C@@]1(O)CC[C@H]2[C@@H]3CCC4=CC(=O)CC[C@]4(C)C3=CC[C@@]21C
Reaction #94828
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(CO)c1ccc(S(=O)(=O)Nc2ccc(Cl)cc2-n2nnc3ncccc32)cc1
Reaction #163194
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C(C)(C)OCC(NS(=O)(=O)c1ccccc1[N+](=O)[O-])(c1cc(Br)ccc1F)C(F)F
Reaction #168766
title compound
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C1CC(S(=O)(=O)c2ccc([N+](=O)[O-])cc2)C(c2ccccc2F)N1C(=O)CNC(=O)Nc1cccc(C(=O)O)c1
Reaction #178074
DOI: 10.1039/C8SC04228D
O=C(NCc1ccc(OC(F)F)cc1)C1CN(c2nc3nc(C(F)(F)F)ncc3s2)CCN1S(=O)(=O)c1ccc(C(F)(F)F)cc1
Reaction #182377
DOI: 10.1039/C8SC04228D
COc1ccc(C=CC(=O)N2CC(CCl)c3c2cc([N+](=O)[O-])c2cc(S(=O)(=O)NCCO)ccc32)cc1
Reaction #185228
DOI: 10.1039/C8SC04228D
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