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41161

CC(C)Oc1ccc(S(C)(=O)=O)cc1C(=O)N1CCN(c2nc3c([N+](=O)[O-])cccc3s2)CC1
Reaction #61434
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.Cl.Oc1ccc2nc(N3CCNCC3COc3cccnc3)sc2c1
Reaction #157394
title compound
Ausbeute 200.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2nc(N3CCN(C(C)=O)CC3COc3cccnc3)sc2c1.Cl.Cl
Reaction #157395
title compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2nc(C(=O)O)cs2)C(COc2cccnc2)C1
Reaction #157398
2-(4-(tert-butoxycarbonyl)-2-((pyridin-3-yloxy)methyl)piperazin-1-yl)thiazole-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)c1csc(N2CCN(C(=O)OC(C)(C)C)CC2COc2cccnc2)n1
Reaction #157399
title compound
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2nc(C(=O)N3CCOCC3)cs2)C(COc2cccnc2)C1
Reaction #157401
title compound
Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.O=C(c1csc(N2CCNCC2COc2cccnc2)n1)N1CCOCC1
Reaction #157402
title compound
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2csc(N3CCNCC3COc3cccnc3)n2)cc1.Cl
Reaction #157404
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2nc(-c3ccc(C(=O)NC4(C(=O)OCc5ccccc5)CCCCC4)cc3)cs2)CC1
Reaction #161048
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2nc(-c3ccc(C(=O)NC4(C(=O)O)CCCCC4)cc3)cs2)CC1
Reaction #161049
title compound
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2nc(-c3ccc(C4=NC5(CCCCC5)C(=O)O4)cc3)cs2)CC1
Reaction #161050
title compound
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1(NC(=O)c2ccc(-c3csc(N4CCN(N5CCOCC5)CC4)n3)cc2)CCCCC1
Reaction #161051
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)COc1ccc(S(C)(=O)=O)cc1C(=O)N1CCN(c2ncc(S(=O)(=O)c3ccccc3)s2)CC1
Reaction #173791
DOI: 10.1039/C8SC04228D
Cc1noc(NC(=O)N2CCN(c3nc(-c4cccc(C(F)(F)F)c4)cs3)CC2)c1C
Reaction #179597
DOI: 10.1039/C8SC04228D
CC(C)Oc1ccc(S(C)(=O)=O)cc1C(=O)N1CCN(c2ncc(CC(F)(F)F)s2)CC1
Reaction #180994
DOI: 10.1039/C8SC04228D
O=C(NO)c1cnc(N2CCN(S(=O)(=O)c3ccc(F)cc3)CC2)s1
Reaction #187022
DOI: 10.1039/C8SC04228D
Cc1cccc(NC(=O)CN2CCN(c3nccs3)CC2)c1
Reaction #189620
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CC2CC1CN2c1nccs1
Reaction #191083
DOI: 10.1039/C8SC04228D
CCSc1cnc(N2CCN(C(=O)OC(C)(C)C)CC2)s1
Reaction #193546
DOI: 10.1039/C8SC04228D
Cc1cccc(-c2csc(N3CCN(C(=O)Nc4onc(C)c4C)CC3)n2)c1
Reaction #194988
DOI: 10.1039/C8SC04228D
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