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1113609

CCc1ccc(I)c2c1CNC2=O
Reaction #49466
7-iodo-4-ethylisoindolinone
Выход 50.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NCc2cccc(I)c21
Reaction #49468
7-iodoisoindolinone
Выход 50.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2ccc(I)c3c2CNC3=O)ccc1O[Si](C)(C)C(C)(C)C
Reaction #49475
7-iodo-4-(4-tert-butyldimethylsilyloxy-3-methoxyphenyl)isoindolinone
Выход 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)Oc1ccc(-c2ccc(I)c3c2CNC3=O)cc1
Reaction #49478
7-iodo-4-(4-tert-butyldimethylsilyloxyphenyl)isoindolinone
Выход 47.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](C)(C)Oc1cccc(-c2ccc(I)c3c2CNC3=O)c1
Reaction #49481
7-iodo-4-(3-tert-butyldimethylsilyloxyphenyl)isoindolinone
Выход 52.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(C(=O)O)[N+](=O)[O-]
Reaction #50745
nitromalonic acid
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
Выход 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
Выход 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
Выход 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
Выход 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
Выход 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
Выход 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
Выход 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(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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