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1412543

[O-][n+]1cc(CN2CCOCC2)ccc1Cl
Reaction #173652
DOI: 10.1039/C8SC04228D
[O-][n+]1cc(CN2CCN(c3ccccc3)CC2)ccc1Cl
Reaction #175107
DOI: 10.1039/C8SC04228D
[O-][n+]1cc(CN2CCCC2)ccc1Cl
Reaction #189889
DOI: 10.1039/C8SC04228D
CC1CCCN(Cc2ccc(Cl)[n+]([O-])c2)C1
Reaction #752724
DOI: 10.1039/C8SC04228D
[O-][n+]1cc(CN2CCOCC2)ccc1Cl
Reaction #835687
title compound
Выход 81.2%DOI: 10.6084/m9.figshare.5104873.v1
[O-][n+]1cc(CN2CCCC2)ccc1Cl
Reaction #835689
title compound
Выход 75.4%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCCN(Cc2ccc(Cl)[n+]([O-])c2)CC1
Reaction #835690
title compound
Выход 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CCN(Cc2ccc(Cl)[n+]([O-])c2)CC1
Reaction #835691
title compound
Выход 56.0%DOI: 10.6084/m9.figshare.5104873.v1
[O-][n+]1cc(CN2CCN(c3ccccc3)CC2)ccc1Cl
Reaction #835692
title compound
Выход 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CCCN(Cc2ccc(Cl)[n+]([O-])c2)C1
Reaction #835693
title compound
Выход 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CCN(Cc2ccc(Cl)[n+]([O-])c2)CC1
Reaction #913665
DOI: 10.1039/C8SC04228D
CCOC(=O)N1CC2CCN(Cc3ccc(Cl)[n+]([O-])c3)C2C1
Reaction #1202834
DOI: 10.1039/C8SC04228D
CN1CCCN(Cc2ccc(Cl)[n+]([O-])c2)CC1
Reaction #1215789
DOI: 10.1039/C8SC04228D
CCN(CC)Cc1ccc(Cl)[n+]([O-])c1
Reaction #1219474
DOI: 10.1039/C8SC04228D
O=[N+]([O-])N=C1NCCN1Cc1ccc(Cl)[n+]([O-])c1
Reaction #1224609
DOI: 10.1039/C8SC04228D
O=[N+]([O-])N=C1NCCN1Cc1ccc(Cl)[n+]([O-])c1
Reaction #1551012
2-chloro-5-(2-nitroimino-imidazolidin-1-yl-methyl)-pyridine-N-oxide
DOI: 10.6084/m9.figshare.5104873.v1
[O-][n+]1cc(CCl)ccc1Cl
Reaction #1656351
DOI: 10.1039/C8SC04228D
[O-][n+]1cc(CCl)ccc1Cl
Reaction #1968515
titled compound
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1C[C@@H]2CCN(Cc3ccc(Cl)[n+]([O-])c3)[C@@H]2C1
Reaction #1968519
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
[O-][n+]1cc(CN2CCOCC2)ccc1Cl
Reaction #2332729
title compound
Выход 81.0%DOI: 10.6084/m9.figshare.5104873.v1
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