2-nitroimidazole

C#CCNC(=O)Cn1ccnc1[N+](=O)[O-]
Reaction #764877
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
O=[N+]([O-])c1nccn1Cc1cn(CCO)nn1
Reaction #1098637
11
Выход 76.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_07
CC(=O)OC(COS(=O)(=O)c1ccc(C)cc1)Cn1cc(Cn2ccnc2[N+](=O)[O-])nn1
Reaction #1098642
16
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_07
CC(=O)OC(COS(=O)(=O)c1ccc(C)cc1)Cn1cc(Cn2ccnc2[N+](=O)[O-])nn1
Reaction #1098643
1-(4-((2-nitro-1H-imidazol-1-yl)methyl)-1H-1,2,3-triazol-1-yl)-3-(tosyloxy)propan-2-yl acetate
Выход 81.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_07
C#CCNC(=O)Cn1ccnc1[N+](=O)[O-]
Reaction #1098646
white solid
Выход 18.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_07
O=[N+]([O-])c1nccn1Cc1cn(C(CO)CF)nn1
Reaction #1098653
1
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_07
O=[N+]([O-])c1nccn1Cc1cn(C(CO)CF)nn1
Reaction #1098654
1
Выход 88.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_07
O=[N+]([O-])c1nccn1Cc1cn(CCO)nn1
Reaction #1244262
11
Выход 76.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_10
CC(=O)OC(COS(=O)(=O)c1ccc(C)cc1)Cn1cc(Cn2ccnc2[N+](=O)[O-])nn1
Reaction #1244267
16
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_10
CC(=O)OC(COS(=O)(=O)c1ccc(C)cc1)Cn1cc(Cn2ccnc2[N+](=O)[O-])nn1
Reaction #1244268
1-(4-((2-nitro-1H-imidazol-1-yl)methyl)-1H-1,2,3-triazol-1-yl)-3-(tosyloxy)propan-2-yl acetate
Выход 81.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_10
C#CCNC(=O)Cn1ccnc1[N+](=O)[O-]
Reaction #1244271
white solid
Выход 18.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_10
O=[N+]([O-])c1nccn1Cc1cn(C(CO)CF)nn1
Reaction #1244278
1
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_10
O=[N+]([O-])c1nccn1Cc1cn(C(CO)CF)nn1
Reaction #1244279
1
Выход 88.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_10