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1337835

COC(=O)[C@H](CO)NC(=O)OCc1ccc([N+](=O)[O-])cc1
Reaction #65541
methyl (2S)-3-hydroxy-2-[(4-nitrobenzyloxycarbonyl)amino]propionate
Выход 24.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccc([N+](=O)[O-])cc1)N1C[C@H](O)C[C@H]1c1nccn1C(=O)OCc1ccc([N+](=O)[O-])cc1
Reaction #65558
(2S, 4R)-4-hydroxy-2-[N-(4-nitrobenzyloxycarbonyl) imidazol-2-yl]-1-(4-nitrobenzyloxycarbonyl) pyrrolidine
Выход 63.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CS[C@H]2C[C@@H](C(=O)O)N(C(=O)OCc3ccc([N+](=O)[O-])cc3)C2)cc1
Reaction #65615
title compound
Выход 77.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CS[C@H]2C[C@@H](C(=O)N3CCN(CCOC(=O)OCc4ccc([N+](=O)[O-])cc4)CC3)N(C(=O)OCc3ccc([N+](=O)[O-])cc3)C2)cc1
Reaction #65619
title compound
Выход 89.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccc([N+](=O)[O-])cc1)Oc1ccc([N+](=O)[O-])cc1
Reaction #83081
desired product
Выход 37.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)[Si](OC[C@H]1O[C@H](CNC(=O)OCc2ccc([N+](=O)[O-])cc2)C[C@@H]1O)(c1ccccc1)c1ccccc1
Reaction #83093
desired product
Выход 75.6%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CCO)c1ccc(N)c(C)c1
Reaction #159262
CD-4
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCNC(=O)OCc1ccc([N+](=O)[O-])cc1
Reaction #175725
DOI: 10.1039/C8SC04228D
CC(C)C(CNC(=O)OCc1ccc([N+](=O)[O-])cc1)NC(=O)OC(C)(C)C
Reaction #180975
DOI: 10.1039/C8SC04228D
CS(=O)(=O)N(CCCl)N(C(=O)OCc1ccc([N+](=O)[O-])cc1)S(C)(=O)=O
Reaction #198556
DOI: 10.1039/C8SC04228D
COc1ccc(CSC2CC(C(=O)N3CC(NC(=O)OCc4ccc([N+](=O)[O-])cc4)C3)N(C(=O)OCc3ccc([N+](=O)[O-])cc3)C2)cc1
Reaction #203369
DOI: 10.1039/C8SC04228D
CC(=NC(=O)OCc1ccc([N+](=O)[O-])cc1)N1CCC(SC(=O)CC2C(C(C)OC(=O)OCc3ccc([N+](=O)[O-])cc3)C(=O)N2C(C(=O)OCc2ccc([N+](=O)[O-])cc2)=C(C)C)C1
Reaction #206895
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCN(C(=O)OCc2ccc([N+](=O)[O-])cc2)CC1
Reaction #230819
DOI: 10.1039/C8SC04228D
O=C(OCc1ccc([N+](=O)[O-])cc1)N1CCC(O)C1
Reaction #231421
DOI: 10.1039/C8SC04228D
O=C(OCc1ccc([N+](=O)[O-])cc1)Oc1ccc([N+](=O)[O-])cc1
Reaction #234001
DOI: 10.1039/C8SC04228D
COc1ccc(CSC2CC(C(=O)N3CCN(CCOC(=O)OCc4ccc([N+](=O)[O-])cc4)CC3)N(C(=O)OCc3ccc([N+](=O)[O-])cc3)C2)cc1
Reaction #272321
DOI: 10.1039/C8SC04228D
CCCC(=O)Nc1cc(C=CC(=O)N2CC(CCl)c3ccc(NC(=O)OCc4ccc([N+](=O)[O-])cc4)cc32)n(C)c1
Reaction #273720
DOI: 10.1039/C8SC04228D
CC(C)=C(C(=O)OCc1ccc([N+](=O)[O-])cc1)N1C(=O)C(C(C)OC(=O)OCc2ccc([N+](=O)[O-])cc2)C1CC(=O)Sc1ccccc1
Reaction #287534
DOI: 10.1039/C8SC04228D
Cc1ccc2c(c1)Nc1c(cnn1C)CN2C(=O)C1CCC(CNC(=O)CC2CCN(C(=O)OCc3ccc([N+](=O)[O-])cc3)CC2)CC1
Reaction #289138
DOI: 10.1039/C8SC04228D
Cc1ccc2c(c1)Nc1c(cnn1C)CN2C(=O)C1CCC(CNC(=O)OCc2ccc([N+](=O)[O-])cc2)CC1
Reaction #307980
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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