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1418769

CC(C)Oc1cc(Nc2nc(Cl)c(Cl)cc2[N+](=O)[O-])n[nH]1
Reaction #163112
title compound
Ausbeute 27.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(Nc2nc(Cl)c([N+](=O)[O-])cc2Cl)n[nH]1
Reaction #163113
title compound
Ausbeute 18.1%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(Cl)c(Cl)nc1Cl
Reaction #266213
DOI: 10.1039/C8SC04228D
CC(C)Oc1cc(Nc2nc(Cl)c(Cl)cc2[N+](=O)[O-])n[nH]1
Reaction #393047
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1cc(Cl)c(Cl)nc1Nc1ccc(CCO)cc1
Reaction #811232
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(Nc2nc(Cl)c([N+](=O)[O-])cc2Cl)n[nH]1
Reaction #907109
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1cc(Cl)c(Cl)nc1Nc1ccc(CCO)cc1
Reaction #945592
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(Cl)c(Cl)nc1Cl
Reaction #1370299
2,5,6-trichloro-3-nitropyridine
Ausbeute 66.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(Nc2nc(Cl)c([N+](=O)[O-])cc2Cl)n[nH]1
Reaction #1524622
title compound
Ausbeute 18.1%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(Cl)c(Cl)nc1Nc1ccc(CCO)cc1
Reaction #1541785
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(Cl)c(Cl)nc1Nc1ccc(CCO)cc1
Reaction #1655862
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1cc(Cl)c(Cl)nc1Nc1ccc(CCO)cc1
Reaction #2164849
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(Nc2nc(Cl)c(Cl)cc2[N+](=O)[O-])n[nH]1
Reaction #2277072
title compound
Ausbeute 27.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(Nc2nc(Cl)c([N+](=O)[O-])cc2Cl)n[nH]1
Reaction #2277073
title compound
Ausbeute 18.1%DOI: 10.6084/m9.figshare.5104873.v1