Recherche de Sous-structure

356381

COC(=O)N(Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1)Cc1cc(I)ccc1-c1cc(C(C)C)ccc1OC
Reaction #45321
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc2c(cnn2C(C)=O)c1
Reaction #50934
methyl 1-acetyl-1H-indazole-5-carboxylate
Rendement 47.4%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
Rendement 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
Rendement 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
Rendement 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
Rendement 60.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCC(=O)N[C@H]1CC[C@H](O[N+](=O)[O-])CC1
Reaction #64246
N-(trans-4-nitroxycyclohexyl)-succinic acid monoamide
Rendement 80.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)CCC(=O)N[C@H]1CC[C@H](O[N+](=O)[O-])CC1
Reaction #64247
N-(trans-4-nitroxycyclohexyl)-succinic acid diamide
Rendement 40.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)N[C@H]1CC[C@H](O[N+](=O)[O-])CC1
Reaction #64248
trans-N-propionyl-4-nitroxycyclohexylamine
Rendement 67.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCCO)N[C@H]1CC[C@H](O[N+](=O)[O-])CC1
Reaction #64249
4-Hydroxy-N-(trans-4-nitroxycyclohexyl)-butyric acid amide
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC[C@@H](C(=O)N[C@H]2CC[C@H](O[N+](=O)[O-])CC2)N1
Reaction #64250
N-(trans-4-nitroxycyclohexyl)-(S)-Pyroglutamic acid amide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cccnc1)[NH+]([O-])[C@H]1CC[C@H](O[N+](=O)[O-])CC1
Reaction #64251
N-(trans-4-nitroxycyclohexyl)-nicotinic acid amide N-oxide
DOI: 10.6084/m9.figshare.5104873.v1
COC1CC(C(=O)O)CC1O[N+](=O)[O-]
Reaction #69429
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC1CC(C(=O)O)CC1O[N+](=O)[O-]
Reaction #69430
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC1CC(C(=O)O)CC1O[N+](=O)[O-]
Reaction #69431
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CC(F)C(O[N+](=O)[O-])C1
Reaction #69432
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CO[C@H]1C[C@@H](C(N)=O)C[C@@H]1O[N+](=O)[O-]
Reaction #69436
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CO[C@H]1C[C@@H](c2n[nH]c(=O)[nH]2)C[C@@H]1O[N+](=O)[O-]
Reaction #69437
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CO[C@H]1C[C@@H](C(=O)NS(=O)(=O)c2ccccc2)C[C@@H]1O[N+](=O)[O-]
Reaction #69438
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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