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1420310

O=[N+]([O-])c1ccc(Oc2cccnc2)c(F)c1
Reaction #41511
3-(2-fluoro-4-nitro-phenoxy)-pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(Oc2ccc([N+](=O)[O-])c(F)c2F)cn1
Reaction #41610
2,3-difluoro-1-(6-methanesulfonyl-pyridin-3-yloxy)-4-nitro-benzene
DOI: 10.6084/m9.figshare.5104873.v1
Nc1noc2cccc(Oc3ccc([N+](=O)[O-])cc3F)c12
Reaction #44675
4-(2-Fluoro-4-nitrophenoxy)-1,2-benzisoxazole-3-amine
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(Oc2cccc3onc(N)c23)c(F)c1
Reaction #44676
4-(4-Amino-2-fluorophenoxy)-1,2-benzisoxazole-3-amine
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(Oc2cccc3occc23)c(F)c1
Reaction #44687
4-(2-Fluoro-4-nitrophenoxy)-1-benzofuran
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(Oc2cccc3occc23)c(F)c1
Reaction #44688
4-(1-Benzofuran-4-yloxy)-3-fluorophenylamine
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(Oc2cc(Cl)ccc2Cl)c(F)c1
Reaction #62036
crude product
Rendimiento 94.7%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(Oc2cc(Cl)ccc2Cl)c(F)c1
Reaction #62037
4-(2,5-Dichloro-phenoxy)-3-fluoro-phenylamine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c([N+](=O)[O-])ccc(OCc2ccccc2)c1F
Reaction #73334
1-benzyloxy-2-fluoro-3-methyl-4-nitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc2[nH]ccc2c1F
Reaction #73335
4-fluoro-1H-indol-5-ol
Rendimiento 52.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(Oc3ccc([N+](=O)[O-])cc3F)ccnc2cc1OCCCN1CCCC1
Reaction #155717
solid
Rendimiento 285.5%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(C2OCCCO2)cnc1-c1cc2nccc(Oc3ccc([N+](=O)[O-])cc3F)c2s1
Reaction #171542
41
Rendimiento 31.2%DOI: 10.6084/m9.figshare.5104873.v1
COCCN(Cc1cnc(-c2cc3nccc(Oc4ccc(N)cc4F)c3s2)n1C)C(=O)OC(C)(C)C
Reaction #171546
title compound 46
Rendimiento 274.9%DOI: 10.6084/m9.figshare.5104873.v1
COCCN(CCn1cc(-c2cc3nccc(Oc4ccc([N+](=O)[O-])cc4F)c3s2)cn1)C(=O)OC(C)(C)C
Reaction #171552
tert-Butyl 2-(4-(7-(2-fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)-1H-pyrazol-1-yl)ethyl(2-methoxyethyl)carbamate
DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)N1CC=C(c2cc3nccc(Oc4ccc([N+](=O)[O-])cc4F)c3s2)CC1
Reaction #171553
title compound 98
Rendimiento 101.1%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc(-c2cc3nccc(Oc4ccc([N+](=O)[O-])cc4F)c3s2)nc1
Reaction #171557
title compound 123
Rendimiento 50.2%DOI: 10.6084/m9.figshare.5104873.v1
COCCNCc1ccc(-c2cc3nccc(Oc4ccc([N+](=O)[O-])cc4F)c3s2)nc1
Reaction #171558
124
Rendimiento 83.9%DOI: 10.6084/m9.figshare.5104873.v1
COCCN(Cc1ccc(-c2cc3nccc(Oc4ccc(N)cc4F)c3s2)nc1)C(=O)OC(C)(C)C
Reaction #171559
title compound 126
Rendimiento 100.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(Oc2ccnc3cc(-c4ccc(C5OCCO5)cn4)sc23)c(F)c1
Reaction #171563
title compound 138
Rendimiento 72.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(Oc2ccnc3cc(-c4ccc(C5OCCO5)cn4)sc23)c(F)c1
Reaction #171564
title compound 139
Rendimiento 95.0%DOI: 10.6084/m9.figshare.5104873.v1
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