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1711

CC(C)(C)OC(=O)N1CCC[C@H]1[C@H](CCOS(C)(=O)=O)C[N+](=O)[O-]
Reaction #1993
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C(=O)c1ccc(OC)cc1)C(CC[N+](=O)[O-])c1ccc2c(c1)OCO2
Reaction #3095
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C(=O)c1ccc(OC)cc1)C(C[N+](=O)[O-])c1ccc2c(c1)OCO2
Reaction #3103
Ethyl 2-(4-methoxybenzoyl)-3-(3,4-methylenedioxy-phenyl)-4-nitro-butanoate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1c2ccccc2CCC1C(Cc1cccc([N+](=O)[O-])c1)[N+](=O)[O-]
Reaction #6488
title compound
Ausbeute 97.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(C(=O)OC(C)(C)C)[C@H](CC[C@H](C[N+](=O)[O-])c1cccc(F)c1F)C(=O)OCc1ccccc1
Reaction #42668
title compound
Ausbeute 87.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(C(=O)OC(C)(C)C)[C@H](CC[C@H](CN)c1cccc(F)c1F)C(=O)O
Reaction #42669
title compound
Ausbeute 97.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(C(=O)OC(C)(C)C)[C@H](CC[C@H](C[N+](=O)[O-])c1cccc(F)c1F)C(=O)OCc1ccccc1
Reaction #48412
title compound
Ausbeute 87.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(C(=O)OC(C)(C)C)[C@H](CC[C@H](CN)c1cccc(F)c1F)C(=O)O
Reaction #48413
title compound
Ausbeute 97.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(C(=O)OC(C)(C)C)[C@H](CC[C@@H](c1cccc(F)c1F)C(CO)[N+](=O)[O-])C(=O)OCc1ccccc1
Reaction #48447
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(C(=O)OC(C)(C)C)[C@H](CC[C@@H](c1cccc(F)c1F)C(N)CO)C(=O)O
Reaction #48448
title compound
Ausbeute 75.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C([C@@H](O)[C@H](Cc2cc(F)cc(F)c2)[N+](=O)[O-])COC1(C)C
Reaction #48610
desired compound
Ausbeute 43.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1[C@@H]([C@@H](O)[C@@H](N)Cc2cc(F)cc(F)c2)COC1(C)C
Reaction #48611
desired compound
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Oc1cccc(C[C@@H]([C@H](O)[C@H]2COC(C)(C)N2C(=O)OC(C)(C)C)[N+](=O)[O-])c1
Reaction #48625
desired compound
Ausbeute 43.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1[C@@H]([C@@H](O)[C@@H](N)Cc2cccc(O)c2)COC1(C)C
Reaction #48626
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(c2ccccc2)(c2ccccc2)OC[C@@H]1[C@@H](O)[C@H](Cc1cc(F)cc(F)c1)[N+](=O)[O-]
Reaction #48675
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(c2ccccc2)(c2ccccc2)OC[C@@H]1[C@@H](O)[C@@H](N)Cc1cc(F)cc(F)c1
Reaction #48676
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1[C@@H]([C@@H](O)[C@H](Cc2cc(F)cc(F)c2)[N+](=O)[O-])COC1(C)C
Reaction #48698
title compound
Ausbeute 37.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1[C@H](OCC(C)(C)C)OC[C@H]([C@@H](O)[C@@H](N)Cc2cc(F)cc(Br)c2)N1C(=O)OC(C)(C)C
Reaction #48738
title compound
Ausbeute 99.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1[C@@H]([C@@H](O)[C@@H](N)Cc2cccc(OC(F)(F)F)c2)COC1(C)C
Reaction #48743
title compound
Ausbeute 92.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)C(=C(SC)SC)[N+](=O)[O-]
Reaction #50508
1-butyroyl-1-nitro-2,2-bis(methylthio)ethylene
DOI: 10.6084/m9.figshare.5104873.v1
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