2-nitroimidazole

C[Si](C)(C)CCOCn1ccnc1[N+](=O)[O-]
Reaction #71340
title compound
المردود 92.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCN(CC)Cc1c[nH]c([N+](=O)[O-])n1
Reaction #71341
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=[N+]([O-])c1nccn1Cc1ccccc1
Reaction #71474
title compound
المردود 50.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)=CCn1ccnc1[N+](=O)[O-]
Reaction #75434
N-(Dimethylallyl)-2-nitroimidazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC(C)=CCCn1ccnc1[N+](=O)[O-]
Reaction #75435
N-(4-Methylpent-3-en-1-yl)-2-nitroimidazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC(C)=CCCn1ccnc1[N+](=O)[O-]
Reaction #75448
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C(OCC1OC(n2ccnc2[N+](=O)[O-])C(OC(=O)c2ccccc2)C1OC(=O)c1ccccc1)c1ccccc1
Reaction #176865
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=[N+]([O-])c1nccn1CCN1CCOCC1
Reaction #193337
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1OCCN1CCn1ccnc1[N+](=O)[O-]
Reaction #221248
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(S(=O)(=O)CCCc2c[nH]c([N+](=O)[O-])n2)cc1
Reaction #232989
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Nc1nccn1C1CCCC1
Reaction #253918
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=[N+]([O-])c1nc(CCc2ccc(B(O)O)cc2)c[nH]1
Reaction #270019
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC(C)=CCCn1ccnc1[N+](=O)[O-]
Reaction #280969
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C1c2ccccc2C(=O)N1CC(O)n1ccnc1[N+](=O)[O-]
Reaction #282948
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=[N+]([O-])c1nccn1C[C@H](O)CCl
Reaction #353898
(S)-(+)-α-(Chloromethyl)-2-nitro-1H-imidazole-1-ethanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
O=[N+]([O-])c1nc(CCc2ccc(B(O)O)cc2)c[nH]1
Reaction #360857
bromide
المردود 14.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_02
CC(C)=CCCn1ccnc1[N+](=O)[O-]
Reaction #365574
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
O=[N+]([O-])c1nccn1C1CCCO1
Reaction #395432
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(=O)OCC(CO)OCn1ccnc1[N+](=O)[O-]
Reaction #439206
1-[1-acetoxymethyl-2-(hydroxy)ethoxy]methyl-2-nitroimidazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
O=CN1CCC(Cn2ccnc2[N+](=O)[O-])CC1
Reaction #451888
4[(2-nitro-1H-imidazol-1-yl)methyl]-1-piperidinecarboxaldehyde
المردود 25.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_08
الصفحة 1التالي