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

CC(C)(N)COc1ccc(O)c(C(N)=O)c1
Reaction #4638
5-(2-amino-2-methylpropoxy)salicylamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(Cc1c[nH]c2c(OCc3ccccc3)cccc12)[N+](=O)[O-]
Reaction #8184
3-(2-methyl-2-nitropropyl)-7-(benzyloxy)indole
Ausbeute 92.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(Cc1c[nH]c2cccc(F)c12)[N+](=O)[O-]
Reaction #8217
4-fluoro-3-(2-methyl-2-nitropropyl)-1H-indole
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc2[nH]cc(CC(C)(C)[N+](=O)[O-])c12
Reaction #8219
3-(2-methyl-2-nitropropyl)-1H-indole-4-carboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(Cc1c[nH]c2c([N+](=O)[O-])cccc12)[N+](=O)[O-]
Reaction #8225
3-(2-nitro-2-methylpropyl)-7-nitroindole
Ausbeute 131.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(Cc1c[nH]c2c(NS(=O)(=O)c3ccccc3)cccc12)[N+](=O)[O-]
Reaction #8226
3-(2-nitro-2-methylpropyl)-7-benzenesulfonamidyl-indole
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(O)C(C)[N+](=O)[O-])cn1.COc1ccc([C@@H](O)[C@H](C)N)cn1
Reaction #41298
subtitle compound 17b
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc(C(F)(C(F)(F)F)C(F)(F)F)cc1
Reaction #48047
4-(1,2,2,2-tetrafluoro-1-trifluoromethyl-ethyl)-benzaldehyde
Ausbeute 30.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)CO[C@H]1CN(C(=O)OC(C)(C)C)[C@@H]([C@@H](O)[C@H](Cc2cc(F)cc(Cl)c2)[N+](=O)[O-])CO1
Reaction #48639
desired compound
Ausbeute 59.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)CO[C@H]1CN(C(=O)OC(C)(C)C)[C@@H]([C@@H](O)[C@@H](N)Cc2cc(F)cc(Cl)c2)CO1
Reaction #48640
desired compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@H](CCC2CCCCC2)OC[C@@H]1[C@@H](O)[C@H](Cc1ccccc1)[N+](=O)[O-]
Reaction #48648
desired compound
Ausbeute 63.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@H](CCC2CCCCC2)OC[C@@H]1[C@@H](O)[C@@H](N)Cc1ccccc1
Reaction #48649
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)CO[C@H]1CN(C(=O)OC(C)(C)C)[C@@H]([C@@H](O)[C@H](Cc2cc(F)cc(F)c2)[N+](=O)[O-])CO1
Reaction #48686
desired compound
Ausbeute 34.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)CO[C@H]1CN(C(=O)OC(C)(C)C)[C@@H]([C@@H](O)[C@@H](N)Cc2cc(F)cc(F)c2)CO1
Reaction #48687
title compound
Ausbeute 78.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1[C@H](OCC(C)(C)C)OC[C@H](C(O)C(N)Cc2cc(F)cc(OCc3ccccc3)c2)N1C(=O)OC(C)(C)C
Reaction #48721
desired compound
Ausbeute 77.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C(SC(=S)N(C)C)c1ccccc1)[N+](=O)[O-]
Reaction #54418
α-(1-nitroethyl)benzyl dimethyldithiocarbamate
DOI: 10.6084/m9.figshare.5104873.v1
COC(c1ccccc1)C(C)([N+](=O)[O-])[N+](=O)[O-]
Reaction #55568
2,2-dinitro-1-methoxy-1-phenylpropane
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC(C)C(CC=C(C)C)[N+](=O)[O-]
Reaction #55924
methyl 3,7-dimethyl-4-nitro-6-octenoate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC(C)C(CC=C(C)C)[N+](=O)[O-]
Reaction #55925
methyl 3,7-dimethyl-4-nitro-6-octenoate
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC(C)C(=O)CC=C(C)C
Reaction #55926
methyl 3,7-dimethyl-4-oxo-6-octenoate
Ausbeute 35.0%DOI: 10.6084/m9.figshare.5104873.v1
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