Substructure Search

17458

O=C1CCCN(C(=O)c2ccc([N+](=O)[O-])cc2)c2ccccc21
Reaction #1435
1-(4-nitrobenzoyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-5-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc2c(c1)OCO2)c1ccc([N+](=O)[O-])cc1
Reaction #2542
title compound
Yield 87.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc([N+](=O)[O-])cc1)N1Cc2nccn2Cc2ccccc21
Reaction #3618
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc([N+](=O)[O-])cc1)N1Cc2cccn2-c2ccccc21
Reaction #3622
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc([N+](=O)[O-])cc1)N1Cc2cccn2Cc2ccoc21
Reaction #3629
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(C(=O)N2Cc3cccn3Cc3ccoc32)cc1
Reaction #3630
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(C(=O)N2Cc3cccn3Cc3ccoc32)cc1
Reaction #3631
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc([N+](=O)[O-])cc1)N1Cc2ccnn2Cc2ccccc21
Reaction #3634
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc([N+](=O)[O-])cc1)N1Cc2cccn2Cc2ccsc21
Reaction #3639
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(C(=O)N2Cc3cccn3Cc3ccsc32)cc1
Reaction #3640
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(C(=O)N2Cc3cccn3Cc3ccsc32)cc1
Reaction #3641
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc([N+](=O)[O-])cc1)N1Cc2cccn2Cc2sccc21
Reaction #3644
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc([N+](=O)[O-])cc1)N1CCc2cccn2-c2ccccc21
Reaction #3648
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc([N+](=O)[O-])cc1)N1CCc2nncn2-c2ccccc21
Reaction #3655
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(C(=O)N2Cc3ccnn3Cc3ccccc32)c(Cl)c1
Reaction #3685
glass
Yield 78.7%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C1CCCN(C(=O)c2ccc([N+](=O)[O-])cc2)c2ccccc21
Reaction #5675
5-dimethylamino-1-(4-nitrobenzoyl)-2,3,4,5-tetrahydro-1H-benzazepine
Yield 97.1%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C1CCCN(C(=O)c2ccc(N)cc2)c2ccccc21
Reaction #5676
5-dimethylamino-1-(4-aminobenzoyl)-2,3,4,5-tetrahydro-1H-benzazepine
Yield 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(O)COC(=O)c1ccc([N+](=O)[O-])cc1
Reaction #8582
title compound
Yield 51.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(N2C(=O)c3cccc(NC(=O)c4ccc([N+](=O)[O-])cc4)c3C2=O)C(=O)N1
Reaction #10106
N-[2-(2,6-Dioxo-piperidin-3-yl)-1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl]-4-nitro-benzamide
Yield 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CN1C(=O)c2ccc([N+](=O)[O-])cc2C1=O)C1(C)OCCO1
Reaction #10949
desired product
Yield 83.2%DOI: 10.6084/m9.figshare.5104873.v1
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