Substructure Search

7176

CCCOc1cc[n+]([O-])c(C)c1C
Reaction #4795
2,3-dimethyl-4-propoxypyridine-1-oxide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c[n+]([O-])c(C)c(C)c1[N+](=O)[O-]
Reaction #59891
title compound
Yield 93.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c[n+]([O-])c(C)c(C)c1Cl
Reaction #59892
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1c([N+](=O)[O-])cc[n+]([O-])c1C
Reaction #59955
title compound
Yield 34.5%DOI: 10.6084/m9.figshare.5104873.v1
CCc1c(Cl)cc[n+]([O-])c1C
Reaction #59956
title compound
Yield 66.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c[n+]([O-])c(C)c(C)c1[N+](=O)[O-]
Reaction #59999
desired product
Yield 81.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c[n+]([O-])c(C)c(C)c1Cl
Reaction #60000
desired product
Yield 83.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c([N+](=O)[O-])cc[n+]([O-])c1CCl
Reaction #63727
2-chloromethyl-3-methyl-4-nitropyridine 1-oxide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c([N+](=O)[O-])cc[n+]([O-])c1C
Reaction #63732
2,3-dimethyl-4-nitropyridine 1-oxide
DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1cc[n+]([O-])c(C)c1C
Reaction #63733
2,3-dimethyl-4-propoxypyridine 1-oxide
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc[n+]([O-])c(C)c1C
Reaction #63743
4-methoxy-2,3-dimethylpyridine 1-oxide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c[n+]([O-])c(C)c(C)c1[N+](=O)[O-]
Reaction #63746
2,3,5-trimethyl-4-nitropyridine 1-oxide
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(C)c[n+]([O-])c(C)c1C
Reaction #63747
4-methoxy-2,3,5-trimethylpyridine 1-oxide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c([N+](=O)[O-])cc[n+]([O-])c1CCl
Reaction #182656
DOI: 10.1039/C8SC04228D
Cc1c(Br)cc[n+]([O-])c1C
Reaction #190406
DOI: 10.1039/C8SC04228D
Cc1c(OCC(F)(F)F)cc[n+]([O-])c1C
Reaction #197374
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c([N+](=O)[O-])c2c([n+]([O-])c1C)CCCCC2
Reaction #227042
DOI: 10.1039/C8SC04228D
CCc1c(Cl)cc[n+]([O-])c1C
Reaction #249757
DOI: 10.1039/C8SC04228D
C=CCOc1c(C)c[n+]([O-])c2c1CCCC2
Reaction #254355
DOI: 10.1039/C8SC04228D
Cc1c(C(F)F)c(Cl)cc[n+]1[O-]
Reaction #269509
DOI: 10.1039/C8SC04228D
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