Substructure Search

10060

O=[N+]([O-])c1ccc(Oc2ccc(F)c(C(F)(F)F)c2)cc1
Reaction #45938
1-fluoro-4-(4-nitrophenoxy)-2-(trifluoromethyl)benzene
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(Oc2ccc(F)c(C(F)(F)F)c2)cc1
Reaction #45962
1-fluoro-4-(4-nitrophenoxy)-2-(trifluoromethyl)benzene
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CNC(C(=O)OC)(C(C)(C)NC(=O)OCc1ccccc1)S(=O)(=O)c1ccc(Oc2ccc(F)cc2)cc1
Reaction #51456
methyl 2(R/S)-[4-(4-fluorophenoxy)benzenesulfonyl][(ethoxycarbonyl)methyl]amino-3-(benzyloxycarbonyl)amino-3-methylbutanoate
Yield 75.1%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(S(=O)(=O)Nc2ncc(Cl)s2)ccc1Oc1ccc(F)cc1-c1cn[nH]c1
Reaction #74514
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Oc1cc([N+](=O)[O-])c(F)cc1Br
Reaction #76770
methyl 2-bromo-4-fluoro-5-nitrophenoxyformate
Yield 97.7%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(O)c(Br)cc1F
Reaction #76771
2-bromo-4-fluoro-5-nitrophenol
Yield 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(Oc2ccc(F)c(F)c2)CCCn2c(-c3ccc(-c4cnc(C)o4)c(OC)c3)nnc21
Reaction #158339
title compound
Yield 44.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(Oc2cc(F)c(F)c(F)c2)CCCn2c(-c3ccc(-c4cnc(C)o4)c(OC)c3)nnc21
Reaction #158340
title compound
Yield 44.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2nnc3n2CCCC3(Oc2cc(F)c(F)c(F)c2)C(C)(C)O)ccc1-c1cnc(C)o1
Reaction #158341
title compound
Yield 117.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1(Oc2ccc(F)c(F)c2)CCCn2c(-c3ccc(-c4cnc(C)o4)c(OC)c3)nnc21
Reaction #158350
title compound
Yield 50.6%DOI: 10.6084/m9.figshare.5104873.v1
CCC(O)(CC)C1(Oc2ccc(F)c(F)c2)CCCn2c(-c3ccc(-c4cnc(C)o4)c(OC)c3)nnc21
Reaction #158351
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC(O)C1(Oc2ccc(F)c(F)c2)CCCn2c(-c3ccc(-c4cnc(C)o4)c(OC)c3)nnc21
Reaction #158352
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2nnc3n2CCCC3(Oc2cc(F)c(F)c(F)c2)C(O)C(F)(F)F)ccc1-c1cnc(C)o1
Reaction #158371
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ncc(-c2ccc(-c3nnc4n3CCCC4(Oc3ccc(F)c(F)c3)C(C)(C)O)cc2O)o1
Reaction #158381
title compound
Yield 137.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cc(-c2nnc3n2CCCC3(Oc2ccc(F)c(F)c2)C(C)(C)O)ccc1-c1cnc(C)o1
Reaction #158382
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(=O)O)c(F)cc1[N+](=O)[O-]
Reaction #174885
DOI: 10.1039/C8SC04228D
CCC(=O)Nc1nc2ccc(Oc3cc(N)c(F)cc3Cl)nc2s1
Reaction #178726
DOI: 10.1039/C8SC04228D
Nc1cc(Oc2ccc3nc(NC(=O)C4CC4)sc3n2)c(Cl)cc1F
Reaction #179345
DOI: 10.1039/C8SC04228D
COc1cc(OCCO)c(F)c(C(Nc2ccc(C(N)=NC(=O)OCC(C)(C)C)cc2)c2nc(OCOC(=O)C(C)(C)C(=O)OC3CCCCC3)n(-c3ncccn3)n2)c1
Reaction #180183
DOI: 10.1039/C8SC04228D
COCCCN1C(=O)COc2ccc(COC3CN(C(=O)OC(C)(C)C)CCC3c3ccc(OCCCOc4ccc(F)cc4)cc3)cc21
Reaction #189873
DOI: 10.1039/C8SC04228D
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