Recherche de Sous-structure

4669

CC(=O)Nc1cc([N+](=O)[O-])c(Cl)cc1F
Reaction #1574
title product
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cc(N)c(Cl)cc1F
Reaction #1575
title product
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(N)c([N+](=O)[O-])cc(-c2ccn(C)c(=O)c2)c1F
Reaction #40529
title compound
Rendement 25.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(F)c(-c2ccccn2)c1
Reaction #41564
compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cc(F)c(OCc2ccccc2)cc1[N+](=O)[O-])c1cnccn1
Reaction #41603
compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cc(Oc2ccccc2F)c(OCc2ccccc2)cc1[N+](=O)[O-])c1cnccn1
Reaction #41604
compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCNc1cc(F)cc(F)c1[N+](=O)[O-]
Reaction #45931
2-butylamino-4,6-difluoronitrobenzene
Rendement 130.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc([N+](=O)[O-])c(F)c(Cl)c1F
Reaction #51443
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)c1cc([N+](=O)[O-])c(F)c(Cl)c1F
Reaction #51444
desired product
DOI: 10.6084/m9.figshare.5104873.v1
C=CCC(C)(C=O)c1cc([N+](=O)[O-])ccc1F
Reaction #59103
2-(2-fluoro-5-nitrophenyl)-2-methylpent-4-enal
DOI: 10.6084/m9.figshare.5104873.v1
CC(CO)(CCO)c1cc([N+](=O)[O-])ccc1F
Reaction #59104
2-(2-fluoro-5-nitrophenyl)-2-methylbutane-1,4-diol
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc([N+](=O)[O-])c(F)c(F)c1F
Reaction #60238
clean desired product
Rendement 92.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1c([N+](=O)[O-])cc(C(=O)O)c(F)c1F
Reaction #60239
pure desired product
Rendement 95.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc([N+](=O)[O-])c(F)c(Cl)c1F
Reaction #60308
clean desired product
Rendement 95.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #61171
1.10
Rendement 37.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1ccc([N+](=O)[O-])c(N2CCCCC2)c1
Reaction #61172
title compound
Rendement 27.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(-n2cccn2)cc1N1CCCCC1
Reaction #61186
title compound
Rendement 85.4%DOI: 10.6084/m9.figshare.5104873.v1
CNc1ccc([N+](=O)[O-])c(N2CCCCC2)c1
Reaction #61188
methyl-(4-nitro-3-piperidin-1-yl-phenyl)-amine
Rendement 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CNc1ccc([N+](=O)[O-])c(N2CCCCC2)c1
Reaction #61191
methyl-(4-nitro-3-piperidin-1-yl-phenyl)-amine
Rendement 100.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@]1(c2cc([N+](=O)[O-])ccc2F)CO[C@@](C)(C(F)(F)F)C(N)=N1
Reaction #67517
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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