Поиск подструктуры

17498

N=C(NCC(=O)N[C@H]1CCNC1)NC(=O)OCc1ccc([N+](=O)[O-])cc1.O=S(=O)(O)OS(=O)(=O)O
Reaction #10041
title compound
Выход 95.4%DOI: 10.6084/m9.figshare.5104873.v1
N=C(NCC(=O)N[C@H]1CCNC1)NC(=O)OCc1ccc([N+](=O)[O-])cc1.O=S(=O)(O)OS(=O)(=O)O
Reaction #1884637
title compound
Выход 95.4%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](NC(=NC(=O)OCc1ccc([N+](=O)[O-])cc1)NC(=O)OCc1ccc([N+](=O)[O-])cc1)C(=O)N[C@H]1CCN(C(=O)OC(C)(C)C)C1
Reaction #2376248
title compound
Выход 100.6%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](NC(=NC(=O)OCc1ccc([N+](=O)[O-])cc1)NC(=O)OCc1ccc([N+](=O)[O-])cc1)C(=O)N[C@H]1CCNC1.O=C(O)C(F)(F)F
Reaction #2376249
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(CC(=O)N[C@H]1CCNC1)C(=NC(=O)OCc1ccc([N+](=O)[O-])cc1)NC(=O)OCc1ccc([N+](=O)[O-])cc1.O=C(O)C(F)(F)F
Reaction #2376254
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(CC(=O)NC1CNC1)C(=NC(=O)OCc1ccc([N+](=O)[O-])cc1)NC(=O)OCc1ccc([N+](=O)[O-])cc1.O=C(O)C(F)(F)F
Reaction #2376256
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC[C@H](NC(=O)CNC(=NC(=O)OCc2ccc([N+](=O)[O-])cc2)NC(=O)OCc2ccc([N+](=O)[O-])cc2)C1
Reaction #2376262
tert-Butyl (3S)-3-[2-[2,3-di(4-nitrobenzyloxycarbonyl)guanidino]acetylamino]-1-pyrrolidinecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CNC(=NC(=O)OCc1ccc([N+](=O)[O-])cc1)NC(=O)OCc1ccc([N+](=O)[O-])cc1)N[C@H]1CCNC1.O=C(O)C(F)(F)F
Reaction #2376263
title compound
DOI: 10.6084/m9.figshare.5104873.v1