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866118

COCOc1cc(CNC(=O)c2cccnc2N)ccc1OCc1ccccc1
Reaction #179919
DOI: 10.1039/C8SC04228D
Nc1ncccc1C(=O)NCc1ccc(Oc2ccc(Cl)cc2)s1
Reaction #213273
DOI: 10.1039/C8SC04228D
Nc1ccc(C(=O)NCc2ccc(Cc3ccccc3)s2)cn1
Reaction #245119
DOI: 10.1039/C8SC04228D
O=C(NCc1ccc(NCc2ccccc2)cc1)c1ccc2ncccc2c1
Reaction #264147
DOI: 10.1039/C8SC04228D
CCS(=O)(=O)N[C@H](C(=O)NCCc1ccc(O)c(OC)c1)C(C)C
Reaction #738159
(S)-2-(ethylsulfonylamino)3-methyl-butyric acid N-[2-(4-hydroxy-3-methoxyphenyl)-ethyl]-amide
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@H](NC(=O)OC(C)(C)C)C(=O)NCCc1ccc(OCc2cccc3ccccc23)c(OC)c1
Reaction #738163
(2S,3S)-2-(tert-butoxy-carbonyl-amino)-3-methyl-valeric acid N-{2-[3-methoxy-4-(naphthalen-1-ylmethoxy)-phenyl]-ethyl}-amide
DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)NC(C(=O)NCCc1ccc(O)c(OC)c1)C(C)C
Reaction #908978
DOI: 10.1039/C8SC04228D
Nc1ccc(C(=O)NCc2ccc(Oc3ccc(F)cc3)s2)cn1
Reaction #911217
DOI: 10.1039/C8SC04228D
O=C(NCc1ccc(Oc2ccccc2)s1)c1cnc2sccc2c1
Reaction #912692
DOI: 10.1039/C8SC04228D
Nc1ccc(C(=O)NCc2ccc(C=CC3CC3)s2)cn1
Reaction #1200356
DOI: 10.1039/C8SC04228D
O=C(NCc1cccc(NCc2ccccc2)c1)c1ccc2ncccc2c1
Reaction #1235913
DOI: 10.1039/C8SC04228D
Nc1ccc(C(=O)NCc2ccc(Oc3ccccc3)s2)cn1
Reaction #1311055
DOI: 10.1039/C8SC04228D
O=C(NCc1ccc(Oc2cccc(F)c2)s1)c1ccc2nccn2c1
Reaction #1655207
DOI: 10.1039/C8SC04228D
Cc1nc(N)ccc1C(=O)Nc1ccc(Oc2cccc(F)c2)s1
Reaction #2167141
6-amino-N-(5-(3-fluoro-phenoxy)-thiophen-2-yl)-methylnicotinamide
Ausbeute 43.9%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(C(=O)NCc2ccc(Cc3ccccc3)s2)cn1
Reaction #2167143
6-amino-N-(5-benzyl-thiophen-2-ylmethyl)-nicotinamide
Ausbeute 29.5%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(C(=O)NCc2ccc(OCc3ccccc3)cc2)cn1
Reaction #2167148
6-amino-N-(4-benzyloxy-benzyl)-nicotinamide
Ausbeute 64.4%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncc([N+](=O)[O-])cc1C(=O)NCc1ccc(Oc2ccccc2)s1
Reaction #2167150
title compound
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CCNC(=O)c1ccc2ncccc2c1
Reaction #2167164
title compound
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1ccc(NCc2ccccc2)cc1)c1ccc2ncccc2c1
Reaction #2167167
title compound
Ausbeute 82.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1ccc(Oc2cccc(F)c2)s1)c1ccc2nccn2c1
Reaction #2167188
title compound
Ausbeute 46.3%DOI: 10.6084/m9.figshare.5104873.v1
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