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O=[N+]([O-])O

N=C(N)Nc1cccc(C(F)(F)F)c1.O=[N+]([O-])O
Reaction #2251
3-trifluoromethyl-phenylguanidine nitrate
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1cccc(Nc2nccc(-c3ccnc(Cl)c3)n2)c1
Reaction #2252
N-(3-trifluoromethyl-phenyl)-4-(2-chloro-4-pyridyl)-2-pyrimidineamine
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #4562
nitro
DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])C(=O)[O-].[Co+2]
Reaction #6402
cobalt oxalate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(Cl)cc1Br
Reaction #7064
title compound
Rendimiento 59.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=[NH2+])Nc1ccccc1.O=[N+]([O-])[O-]
Reaction #8589
N-phenylguanidinium nitrate
Rendimiento 32.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(-c2nn3c(NC4CCCC4)cccc3c2-c2ccnc(Nc3ccccc3)n2)cc1
Reaction #8590
3-(2-anilino-4-pyrimidinyl)-N-cyclopentyl-2-(4-fluorophenyl)pyrazolo[1,5-α]pyridin-7-amine
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(-c2nn3ccc(Cl)cc3c2-c2ccnc(Nc3ccccc3)n2)cc1
Reaction #8605
4-[5-chloro-2-(4-fluorophenyl)pyrazolo[1,5-α]pyridin-3-yl]-N-phenyl-2-pyrimidinamine
Rendimiento 36.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(Cl)cc2c1[nH]c1cncc(F)c12
Reaction #40514
6-chloro-4-fluoro-8-nitro-9H-β-carboline
Rendimiento 102.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc([N+](=O)[O-])cc1NC(=N)N
Reaction #42045
objective compound
Rendimiento 100.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cccc(I)c1C(=O)O
Reaction #49388
3-iodophthalic acid
Rendimiento 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](NC(=O)OCc1ccccc1)C(=O)NCCCN[C@H](C(=O)OC(C)(C)C)[C@@H](O)C1O[C@@H](n2ccc(=O)[nH]c2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C
Reaction #53990
tert-butyl (5S,12S)-12-[(R)-[(3R,4R,5R)-3,4-bis{[tert-butyl(dimethyl)silyl]oxy}-5-(2,4-dioxo -3,4-dihydro-1(2H)-pyrimidinyl)tetrahydro-2-furanyl](hydroxy)methyl]-5-isobutyl-3,6-dioxo-1-phenyl-2-oxa-4,7,11-triazatridecan-13-oate
Rendimiento 25.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #60639
3-Dimethylamino-1-(2-ethylamino-4-methyl-thiazol-5-yl)-propenone
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1ccc(Nc2cc(-c3ccc(Cl)cc3)ccn2)cc1
Reaction #61724
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)O[C@H](C)[C@H]1C(=O)N[C@@H]1OC(C)=O
Reaction #62561
(3R,4R)-3-[(1R)-1-allyloxycarbonyloxyethyl]-4-acetoxy-2-azetidinone
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@H]1CC[C@H](O[N+](=O)[O-])CC1
Reaction #64241
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@H]1CC[C@H](O[N+](=O)[O-])CC1
Reaction #64242
trans-N-acetyl-4-nitroxycyclohexylamine
Rendimiento 53.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@H]1CC[C@H](O[N+](=O)[O-])CC1
Reaction #64243
trans-N-acetyl-4-nitroxycyclohexylamine
Rendimiento 35.0%DOI: 10.6084/m9.figshare.5104873.v1
O=CN[C@H]1CC[C@H](O[N+](=O)[O-])CC1
Reaction #64244
title compound
Rendimiento 66.4%DOI: 10.6084/m9.figshare.5104873.v1
O=CN[C@H]1CC[C@H](O[N+](=O)[O-])CC1
Reaction #64245
trans-N-formyl-4-nitroxycyclohexylamine
Rendimiento 60.0%DOI: 10.6084/m9.figshare.5104873.v1
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