Substructure Search

Nc1ccc(I)cc1N

O=c1[nH]c2ccc(I)cc2[nH]c1=O
Reaction #82626
title compound
Yield 78.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cc(Nc2ccc(I)cc2[N+](=O)[O-])cc(-n2cccc2)c1
Reaction #92392
N-(3-(4-iodo-2-nitrophenylamino)-5-(1H-pyrrol-1-yl)phenyl)acetamide
Yield 49.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Nc1cc(Cl)c(C#Cc2ccccc2)cc1[N+](=O)[O-]
Reaction #173343
DOI: 10.1039/C8SC04228D
COc1ccc(C#Cc2ccc3c(c2)NC(=O)CC(c2cccc(C#N)c2)=N3)cc1
Reaction #176223
DOI: 10.1039/C8SC04228D
CN(CCO)c1cc(NC(=O)OC(C)(C)C)c([N+](=O)[O-])cc1I
Reaction #176711
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)Nc1ccc(-c2ccc(F)cc2F)cc1[N+](=O)[O-]
Reaction #182869
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)Nc1ccc(-c2cccc(F)c2F)cc1[N+](=O)[O-]
Reaction #184674
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)Nc1cc(CO)c(C#Cc2ccccc2)cc1[N+](=O)[O-]
Reaction #192549
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1cc(I)ccc1Nc1cccc(-c2cncnc2)c1
Reaction #195712
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)Nc1ccc(-c2ccncc2)cc1[N+](=O)[O-]
Reaction #201232
DOI: 10.1039/C8SC04228D
CN1CCN(c2cc(NC(=O)OC(C)(C)C)c([N+](=O)[O-])cc2C#Cc2ccccc2)CC1
Reaction #207649
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)Nc1ccc(-c2cccc(F)c2)cc1[N+](=O)[O-]
Reaction #209695
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)Nc1cc(OCC#N)c(C#Cc2ccccc2)cc1[N+](=O)[O-]
Reaction #221339
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)Nc1ccc(-c2cccnc2)cc1[N+](=O)[O-]
Reaction #224360
DOI: 10.1039/C8SC04228D
COCCOc1cc(NC(=O)OC(C)(C)C)c([N+](=O)[O-])cc1-c1ccccc1F
Reaction #229674
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)Nc1cc(N2CCC3(CC2)OCCO3)c(-c2ccccc2F)cc1[N+](=O)[O-]
Reaction #230075
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)Nc1ccc(-c2cccs2)cc1[N+](=O)[O-]
Reaction #238580
DOI: 10.1039/C8SC04228D
COc1cccc(F)c1-c1ccc(NC(=O)OC(C)(C)C)c([N+](=O)[O-])c1
Reaction #239071
DOI: 10.1039/C8SC04228D
N#Cc1cccc(C2=Nc3cc(N4CCSCC4)c(C#Cc4ccccc4)cc3NC(=O)C2)c1
Reaction #241811
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)Nc1cc(COC2CCCCO2)c(-c2ccccc2F)cc1[N+](=O)[O-]
Reaction #260453
DOI: 10.1039/C8SC04228D
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