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Cc1c(Br)c(F)c([N+](=O)[O-])c(N)c1C#N
Reaction #45829
2-Amino-5-bromo-4-fluoro-6-methyl-3-nitrobenzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Br)c(N2CC[C@H](N(C)C)C2)c([N+](=O)[O-])c(N)c1C#N
Reaction #45830
compound
Ausbeute 97.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C#N)c(N)c([N+](=O)[O-])c(N2CC[C@H](N(C)C)C2)c1-c1ccccc1
Reaction #45831
compound
Ausbeute 90.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C#N)c(N)c(N)c(N2CC[C@H](N(C)C)C2)c1-c1ccccc1
Reaction #45832
compound
Ausbeute 97.3%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C(=O)N[C@H]1C=C2c3ccc([N+](=O)[O-])c4[nH]cc(c34)C[C@H]2N(C)C1
Reaction #63492
3-(9,10-didehydro-6-methyl-14-nitro-8α-ergolinyl)-1,1-diethylurea
Ausbeute 46.9%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCc2c(N)c([N+](=O)[O-])cc(Br)c2C1
Reaction #76481
title compound
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCc2c(N)c(N)cc(Br)c2C1
Reaction #76482
title compound
Ausbeute 90.1%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCc2c(ccc(N)c2N)C1
Reaction #76483
title compound
Ausbeute 48.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCN1CCc2c(ccc(N)c2N)C1
Reaction #76484
title compound
Ausbeute 129.7%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCc2c(Br)cc(N)c(N)c2C1
Reaction #76500
5-Bromo-1,2,3,4-tetrahydro-2-methyl-7,8-isoquinolinediamine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N)c([N+](=O)[O-])cc2c1C(=O)N(CCN(C)C)C2=O
Reaction #156537
designed compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N)c(N)cc2c1C(=O)N(CCN(C)C)C2=O
Reaction #156538
5,6-Diamino-2-(2-(dimethylamino)ethyl)-4-methylisoindoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(Br)c2c(c1N)CN(CCCc1ccccc1)CC2
Reaction #180378
DOI: 10.1039/C8SC04228D
CCOC(=O)C(=O)Nc1c([N+](=O)[O-])cc(S(=O)(=O)NC(=O)C(=O)OCC)c2c1CCCC2
Reaction #190583
DOI: 10.1039/C8SC04228D
CC(=O)c1cc([N+](=O)[O-])c(N)c2c1CCCC2
Reaction #234512
DOI: 10.1039/C8SC04228D
CCOC(=O)C1(c2ccc([N+](=O)[O-])c(NC)c2C#N)CCCC1=O
Reaction #245953
DOI: 10.1039/C8SC04228D
Nc1cc(Br)c2c(c1N)CN(CCc1ccccc1)CC2
Reaction #270986
DOI: 10.1039/C8SC04228D
Nc1cc(Br)c2c(c1N)CN(Cc1ccccc1)CC2
Reaction #296235
DOI: 10.1039/C8SC04228D
COC(=O)c1c(C(=O)O)cc([N+](=O)[O-])c(N)c1C
Reaction #297072
DOI: 10.1039/C8SC04228D
O=C1c2cccc([N+](=O)[O-])c2C(=O)c2cccc([N+](=O)[O-])c21
Reaction #324031
1,5-dinitroanthraquinone
DOI: 10.6084/m9.figshare.5104873.v1
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