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804645

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
Ausbeute 95.4%DOI: 10.6084/m9.figshare.5104873.v1
CN1C[C@@H](S)C[C@H]1C(=O)N1CC[C@H](NC(=O)OCc2ccc([N+](=O)[O-])cc2)C1
Reaction #449234
title compound
Ausbeute 71.6%DOI: 10.6084/m9.figshare.5104873.v1
CN1C[C@@H](S)C[C@H]1C(=O)N1CC(NC(=O)OCc2ccc([N+](=O)[O-])cc2)C1
Reaction #449294
title compound
Ausbeute 75.1%DOI: 10.6084/m9.figshare.5104873.v1
CN1C[C@@H](S)C[C@H]1C(=O)N1CC(NC(=N)CC(=O)OCc2ccc([N+](=O)[O-])cc2)C1
Reaction #449295
title compound
Ausbeute 93.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=C(S[C@H]3C[C@@H](C(=O)N4CC[C@H](NC(=O)CNC(=NC(=O)OCc5ccc([N+](=O)[O-])cc5)NC(=O)OCc5ccc([N+](=O)[O-])cc5)C4)N(C)C3)[C@H](C)[C@H]12
Reaction #671276
desired compound
Ausbeute 66.1%DOI: 10.6084/m9.figshare.5104873.v1
CN1C[C@@H](S)C[C@H]1C(=O)N1CC[C@H](NC(=O)CNC(=N)NC(=O)OCc2ccc([N+](=O)[O-])cc2)C1
Reaction #671277
(2S,4S)-4-mercapto-1-methyl-2-[(3S)-3[2-[3-(4-nitrobenzyloxycarbonyl)guanidino]acetylamino]pyrrolidin-1-yl-carbonyl]pyrrolidine
Ausbeute 58.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1CCN(C(=O)C2CC(S)CN2C(=O)OCc2ccc([N+](=O)[O-])cc2)C1)OCc1ccc([N+](=O)[O-])cc1
Reaction #767669
DOI: 10.1039/C8SC04228D
O=C(N[C@H]1CCN(C(=O)[C@@H]2C[C@H](S)CN2C(=O)OCc2ccc([N+](=O)[O-])cc2)C1)OCc1ccc([N+](=O)[O-])cc1
Reaction #814820
title compound
Ausbeute 103.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CCN(C(=O)[C@@H]2C[C@H](S)CN2C(=O)OCc2ccc([N+](=O)[O-])cc2)C1)OCc1ccc([N+](=O)[O-])cc1
Reaction #814836
title compound
Ausbeute 65.8%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=C(S[C@H]3C[C@@H](C(=O)N4CCN(C(=N)NC(=O)OCc5ccc([N+](=O)[O-])cc5)CC4)N(C)C3)[C@H](C)[C@H]12
Reaction #814881
title compound
Ausbeute 76.9%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)O)=C(S[C@H]3C[C@@H](C(=O)N4CC[C@H](NC(=N)N)C4)N(C)C3)[C@H](C)[C@H]12
Reaction #814885
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)O)=C(S[C@@H]3CN[C@H](C(=O)NC4CCN(C(=N)N)CC4)C3)[C@H](C)[C@H]12
Reaction #814890
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1C[C@@H](S)C[C@H]1C(=O)N1CC(NC(=O)OCc2ccc([N+](=O)[O-])cc2)C1
Reaction #814908
title compound
Ausbeute 75.1%DOI: 10.6084/m9.figshare.5104873.v1
CN1CC(S)CC1C(=O)N1CC(NC(=N)CC(=O)OCc2ccc([N+](=O)[O-])cc2)C1
Reaction #814909
title compound
Ausbeute 93.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CSC2CC(C(=O)N3CCC(NC(=O)CNC(=NC(=O)OCc4ccc([N+](=O)[O-])cc4)NC(=O)OCc4ccc([N+](=O)[O-])cc4)C3)N(C)C2)cc1
Reaction #911314
DOI: 10.1039/C8SC04228D
CN1CC(S)CC1C(=O)N1CCC(NC(=O)CNC(=NC(=O)OCc2ccc([N+](=O)[O-])cc2)NC(=O)OCc2ccc([N+](=O)[O-])cc2)C1
Reaction #919162
DOI: 10.1039/C8SC04228D
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=C(S[C@H]3C[C@@H](C(=O)N4CC[C@H](NC(=O)OCc5ccc([N+](=O)[O-])cc5)C4)N(C)C3)[C@H](C)[C@H]12
Reaction #950534
title compound
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CC(S)CC1C(=O)N1CCC(NC(=O)CNC(=N)NC(=O)OCc2ccc([N+](=O)[O-])cc2)C1
Reaction #1309579
DOI: 10.1039/C8SC04228D
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)OCc3ccc([N+](=O)[O-])cc3)=C(S[C@H]3C[C@@H](C(=O)N4CC[C@H](NC(=O)OCc5ccc([N+](=O)[O-])cc5)C4)N(C)C3)[C@H](C)[C@H]12
Reaction #1577543
title compound
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CC(S)CC1C(=O)N1CC(NC(=O)OCc2ccc([N+](=O)[O-])cc2)C1
Reaction #1662384
DOI: 10.1039/C8SC04228D
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