Recherche de Sous-structure

547626

C[C@H](Nc1nc(Nc2cc(C3CC3)[nH]n2)c(F)cc1[N+](=O)[O-])c1ccc(F)cc1
Reaction #163069
title compound
Rendement 66.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(Nc2nc(N[C@@H](C)c3ccc(F)cc3)c([N+](=O)[O-])cc2F)n[nH]1
Reaction #163070
title compound
Rendement 40.6%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(F)c(F)nc1N[C@H](CO)c1ccc(F)cc1
Reaction #163111
(S)-2-(5,6-Difluoro-3-nitropyridin-2-ylamino)-2-(4-fluorophenyl)ethanol
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(F)c(F)nc1NC(CO)c1ccc(F)cc1
Reaction #890586
DOI: 10.1039/C8SC04228D
CC(Nc1nc(Nc2cc(C3CC3)[nH]n2)c(F)cc1[N+](=O)[O-])c1ccc(F)cc1
Reaction #1026517
DOI: 10.1039/C8SC04228D
CC(Nc1nc(F)c(F)cc1[N+](=O)[O-])c1ccc(F)cc1
Reaction #1222378
DOI: 10.1039/C8SC04228D
Cc1cc(Nc2nc(NC(C)c3ccc(F)cc3)c([N+](=O)[O-])cc2F)n[nH]1
Reaction #1326332
DOI: 10.1039/C8SC04228D
Cc1cc(Nc2nc(N[C@@H](C)c3ccc(F)cc3)c([N+](=O)[O-])cc2F)n[nH]1
Reaction #1524618
title compound
Rendement 69.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Nc1nc(F)c(F)cc1[N+](=O)[O-])c1ccc(F)cc1
Reaction #1524619
title compound
Rendement 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(Nc2nc(NC(C)c3ccc(F)cc3)c([N+](=O)[O-])cc2F)n[nH]1
Reaction #1649079
DOI: 10.1039/C8SC04228D
C[C@H](Nc1nc(Nc2cc(C3CC3)[nH]n2)c(F)cc1[N+](=O)[O-])c1ccc(F)cc1
Reaction #2277032
title compound
Rendement 66.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(Nc2nc(N[C@@H](C)c3ccc(F)cc3)c([N+](=O)[O-])cc2F)n[nH]1
Reaction #2277033
title compound
Rendement 40.6%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(F)c(F)nc1N[C@H](CO)c1ccc(F)cc1
Reaction #2277071
title compound
Rendement 57.2%DOI: 10.6084/m9.figshare.5104873.v1