Recherche de Sous-structure

18836

C=CCN(C(=O)OCc1ccccc1)c1cnc2n(c1=O)[C@H](C(=O)Nc1ccccc1)C[C@@]2(C)N=[N+]=[N-]
Reaction #11065
azide
Rendement 65.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](c1ccccc1)[C@H](N=[N+]=[N-])C(=O)N1C(=O)OC[C@@H]1c1ccccc1
Reaction #61115
(S)-3-((2S,3R)-2-azido-3-phenyl-butyryl)-4-phenyl-oxazolidin-2-one
Rendement 41.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(c1ccccc1)[C@H](N=[N+]=[N-])C(=O)N1C(=O)OC[C@@H]1Cc1ccccc1
Reaction #221024
colored oil
Rendement 96.9%DOI: 10.6084/m9.figshare.5104873.v1
CN1N=Cc2ccccc2C(N=[N+]=[N-])C1=O
Reaction #225987
DOI: 10.1039/C8SC04228D
[N-]=[N+]=NC1N=C(c2ccccc2)c2cccc(Cl)c2N(CC(F)(F)F)C1=O
Reaction #256391
DOI: 10.1039/C8SC04228D
[N-]=[N+]=NC(C(=O)N1C(=O)OCC1Cc1ccccc1)C(c1ccc(Cl)cc1)c1ccc(Cl)cc1
Reaction #273813
DOI: 10.1039/C8SC04228D
CC1(N=[N+]=[N-])CCCCn2c1nc(-c1ccncn1)cc2=O
Reaction #305076
10-azido-1 0-methyl-2-pyrimidin-4-yl-7,8,9,10-tetrahydro-6H-pyrimido[1,2-a]azepin-4-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cc(C(C)C)c(S(=O)(=O)N=[N+]=[N-])c(C(C)C)c1
Reaction #345389
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(CN2C(=O)c3ccccc3N(CC(F)(F)F)C(=O)C2N=[N+]=[N-])c(OC)c1
Reaction #377485
DOI: 10.1039/C8SC04228D
C[C@@H]1C[C@@H](N=[N+]=[N-])C(=O)N1Cc1ccccc1
Reaction #409706
13-4
DOI: 10.6084/m9.figshare.5104873.v1
CCN1C=C(N=[N+]=[N-])N=C(C2CC2)c2ccccc21
Reaction #410762
powder
Rendement 82.2%DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=NC1CC(c2cccc(F)c2F)CN(CC(F)(F)F)C1=O
Reaction #422045
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1C(c2cc(F)cc(F)c2F)CC(N=[N+]=[N-])C(=O)N1CC(F)(F)F
Reaction #422051
title compound
DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=NC1CC(c2cccc(F)c2F)CN(CC(F)(F)F)C1=O
Reaction #493743
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1C(c2cc(F)cc(F)c2F)CC(N=[N+]=[N-])C(=O)N1CC(F)(F)F
Reaction #493749
title compound
DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=NC1CC(c2cccc(F)c2F)CN(CC(F)(F)F)C1=O
Reaction #535421
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1C(c2cc(F)cc(F)c2F)CC(N=[N+]=[N-])C(=O)N1CC(F)(F)F
Reaction #535427
title compound
DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=NC1N=C(c2ccccc2)c2cccc(Cl)c2N(CC(F)(F)F)C1=O
Reaction #547077
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@]1(N=[N+]=[N-])C[C@@H](C(=O)Nc2ccccc2)n2c1ncc(N(Cc1cccc(C(F)(F)F)c1)C(=O)OCc1ccccc1)c2=O
Reaction #568431
azide
Rendement 71.3%DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=N[C@H](C(=O)N1C(=O)OC[C@@H]1c1ccccc1)[C@@H](c1ccc(F)cc1)c1cc(F)cc(F)c1
Reaction #716936
(4S)-3-[(2S,3S)-2-Azido-3-(3,5-difluorophenyl)-3-(4-fluorophenyl)propanoyl]-4-phenyl-1,3-oxazolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
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