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8977

Cc1cc([N+](=O)[O-])c(F)c[n+]1[O-]
Reaction #1953
title compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCCc1cc[n+]([O-])cc1
Reaction #11573
titled compound
Ausbeute 94.2%DOI: 10.6084/m9.figshare.5104873.v1
[O-][n+]1ccc(OCc2ccccc2)cc1
Reaction #43307
title compound
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #63730
2-[[5-amino-1,3,4-thiadiazol-2 -yl)dithio]methyl
DOI: 10.6084/m9.figshare.5104873.v1
COc1c[n+]([O-])ccc1N
Reaction #63787
4-amino-3-methoxy-pyridine-N-oxide
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc[n+]([O-])c2ccccc12
Reaction #68007
4-methoxyquinoline N-oxide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(C[n+]1ccccc1)c1ccccc1.[Br-]
Reaction #75290
N-phenacylpyridinium bromide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(C[n+]1ccccc1)c1ccccc1.[Br-]
Reaction #75291
N-phenacylpyridinium bromide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2c(Cl)c3ccccc3[n+](CCCN3C(=O)c4ccccc4C3=O)c2c1C.[Cl-]
Reaction #76465
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(ccc[n+]2[O-])c1
Reaction #84108
6-methoxyquinoline 1-oxide
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2nc(O)ccc2c1
Reaction #84109
6-methoxyquinolin-2-ol
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O[C@@H](Cc1c(Cl)c[n+]([O-])cc1Cl)c1ccc(OC(F)F)c(O)c1)c1cccs1
Reaction #88041
(S)-3,5-dichloro-4-(2-(4-(difluoromethoxy)-3-hydroxyphenyl)-2-(thiophene-2-carbonyloxy)ethyl)pyridine 1-oxide
Ausbeute 41.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc(Br)c[n+]([O-])c1)N1CCc2cc(F)ccc21
Reaction #161774
3-bromo-5-(5-fluoroindoline-1-carbonyl)pyridine-1-oxide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)CCN(C1CCN(c3cc(C(=O)N4CCc5cc(F)ccc54)c[n+]([O-])c3)CC1)C(=O)N2
Reaction #161860
3-(5-fluoroindoline-1-carbonyl)-5-(4-(7-methoxy-2-oxo-4,5-dihydro-1H-benzo[d][1,3]-diazepin-3(2H)-yl)piperidin-1-yl)pyridine-1-oxide
DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])c1cccc(Cl)c1.O[n+]1cccc2cc[nH]c21
Reaction #166689
7-hydroxy-1H-pyrrolo[2,3-b]pyridin-7-ium 3-chlorobenzoate
Ausbeute 89.4%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccnc2[nH]ccc12
Reaction #166690
4-chloro-1H-pyrrolo[2,3-b]pyridine
Ausbeute 57.8%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1c(Cl)c[n+]([O-])cc1-c1ccc(Oc2ccccc2)cc1
Reaction #168217
3-chloro-4-cyano-5-(4-phenoxyphenyl)pyridine 1-oxide
Ausbeute 63.1%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1c(-c2ccc(Oc3ccccc3)cc2)cnc(Cl)c1Cl
Reaction #168218
2,3-dichloro-5-(4-phenoxyphenyl)isonicotinonitrile
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-c2c[n+]([O-])cc(Cl)c2C#N)c1
Reaction #168226
3-chloro-4-cyano-5-(3-methoxyphenyl)pyridine 1-oxide
Ausbeute 93.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-c2cnc(Cl)c(Cl)c2C#N)c1
Reaction #168227
2,3-dichloro-5-(3-methoxyphenyl)isonicotinonitrile
DOI: 10.6084/m9.figshare.5104873.v1
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