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Cc1nc(-c2ccc(N)cc2)no1

FC(F)(F)c1sc(-c2nc(-c3ccc4c(c3)CCN4)no2)cc1-c1ccccc1
Reaction #69399
3-(indolin-5-yl)-5-(4-phenyl-5-(trifluoromethyl)thiophen-2-yl)-1,2,4-oxadiazole
Ausbeute 84.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nc(-c2ccc([N+](=O)[O-])cc2)no1
Reaction #82821
5-ethoxycarbonyl-3-(4-nitrophenyl)-1,2,4-oxadiazole
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(NC(=O)c1nc(-c2ccc(NC(=O)Nc3ccc(F)cc3F)cc2)no1)C(C)C
Reaction #162995
Methyl 2-(3-(4-(3-(2,4-difluorophenyl) ureido)phenyl)-1,2,4-oxadiazole-5-carboxamido)-3-methylbutanoate
Ausbeute 98.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CNCc2nc(-c3ccc(N4CCC(N(C)C)C4)cc3)no2)cc1
Reaction #174021
DOI: 10.1039/C8SC04228D
COc1cc(C(C#N)Nc2ccc(-c3noc(C)n3)cc2)cc(CO[Si](C(C)C)(C(C)C)C(C)C)c1OC
Reaction #186331
DOI: 10.1039/C8SC04228D
COc1cc(C(C#N)Nc2ccc(-c3noc(C)n3)cc2)cc2c1OCCC2
Reaction #202784
DOI: 10.1039/C8SC04228D
Nc1ccc(-c2noc(C3CCCCN3C(=O)COc3ccccc3)n2)cc1
Reaction #204713
DOI: 10.1039/C8SC04228D
Nc1ccc(-c2noc(-c3ccc(OC(F)(F)F)cc3)n2)cc1
Reaction #239032
DOI: 10.1039/C8SC04228D
COc1cc(C(C#N)Nc2ccc(-c3noc(C)n3)cc2)c(F)c2c1OCOC2
Reaction #249708
DOI: 10.1039/C8SC04228D
COc1cc(C(C#N)Nc2ccc(-c3noc(C)n3)cc2)cc(C(C)O[Si](C(C)C)(C(C)C)C(C)C)c1OC
Reaction #258334
DOI: 10.1039/C8SC04228D
COc1cc(OCCF)c(F)c(C(Nc2ccc(-c3noc(C)n3)cc2)c2nn(-c3cccc(N)n3)c(=O)[nH]2)c1
Reaction #259361
DOI: 10.1039/C8SC04228D
COc1cc(C(C#N)Nc2ccc(-c3noc(C)n3)cc2)cc2c1OCOC2
Reaction #259742
DOI: 10.1039/C8SC04228D
COc1cc(C(C#N)Nc2ccc(-c3noc(C)n3)cc2)cc2c1OCC2
Reaction #259891
DOI: 10.1039/C8SC04228D
COC(=O)N=C(SC)C(=Nc1ccc(-c2noc(C)n2)cc1)c1cc(OC)cc(OCCO[Si](C)(C)C(C)(C)C)c1F
Reaction #265623
DOI: 10.1039/C8SC04228D
CC(=O)O
Reaction #265782
DOI: 10.1039/C8SC04228D
Cc1nc(-c2ccc(Nc3nc(NC4CCCCC4N)ncc3C(N)=O)cc2)no1
Reaction #273706
DOI: 10.1039/C8SC04228D
Cc1nc(-c2ccc(N3CC(CO)OC3=O)cc2)no1
Reaction #283283
DOI: 10.1039/C8SC04228D
Cc1nc(-c2ccc(NC(=O)N3CCNCC3)cc2)no1
Reaction #293240
DOI: 10.1039/C8SC04228D
CCC(CC)c1cc(-c2nc(-c3cc(C)c(NS(C)(=O)=O)c(Cl)c3)no2)cc(OC)n1
Reaction #332291
title compound
Ausbeute 57.8%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc(-c2noc(-c3cc(OC)nc(C(CC)CC)c3)n2)cc(C)c1NS(C)(=O)=O
Reaction #332295
title compound
Ausbeute 36.6%DOI: 10.6084/m9.figshare.5104873.v1
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