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CNc1cc(OC)c(C(=O)[NH+]([O-])C2CN3CCC2CC3)cc1Cl.Cl
Reaction #3859
N-oxide
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(N)c(Cl)cc1C(=O)CCCCCl
Reaction #250328
DOI: 10.1039/C8SC04228D
COc1cc(N)c(Cl)cc1C(C)=O
Reaction #296652
DOI: 10.1039/C8SC04228D
COc1cc(NC(C)=O)c(Cl)cc1C(=O)[NH+]([O-])C1CCN(CC2CCCCC2)CC1
Reaction #348239
N-(1-cyclohexylmethylpiperid-4-yl)-2-methoxy-4-acetamido-5-chlorobenzamide N-oxide
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(NC(C)=O)c(Cl)cc1C(=O)[NH+]([O-])C1CCN(CC2CCCCC2)CC1
Reaction #389314
DOI: 10.1039/C8SC04228D
COc1cc(N)ccc1C(=O)NO
Reaction #400037
DOI: 10.1039/C8SC04228D
O=C(NO)c1ccccc1O
Reaction #450343
Sepharose
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(C(=O)OC(C)(C)C)CC1
Reaction #887391
DOI: 10.1039/C8SC04228D
COc1cc(N)c(Cl)cc1C(=O)N(C)OC
Reaction #1050518
N-methoxy-N-methyl-4-amino-5-chloro-2-methoxybenzamide
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(C(=O)OC(C)(C)C)CC1
Reaction #1050519
1-(4-amino-5-chloro-2-methoxyphenyl)-3-[1-(tert-butoxycarbonyl)piperidin-4-yl]-propan-1-one
Ausbeute 21.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(N)c(Cl)cc1C(C)=O
Reaction #1050541
4'-amino-5'-chloro-2'-methoxyacetophenone
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(N)c(Cl)cc1C(=O)CCCCCl
Reaction #1050558
1-(4-amino-5-chloro-2-methoxyphenyl)-5-chloropentan-1-one
Ausbeute 81.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NO)c1ccccc1O
Reaction #1078322
Sepharose
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(N)ccc1C(=O)NO
Reaction #1183759
title compound
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cc(OCC2CC2)c(C(=O)[NH+]([O-])C2CN3CCC2CC3)cc1Cl
Reaction #1210930
DOI: 10.1039/C8SC04228D
O=C(NO)c1ccccc1O
Reaction #1687589
Sepharose
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cc(N)c(Cl)cc1C(=O)[NH+]([O-])CC1CN(Cc2ccccc2Cl)CCO1
Reaction #1695386
title compound
Ausbeute 14.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NO)c1ccccc1O
Reaction #2042543
Sepharose
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(N)ccc1C(=O)NO
Reaction #2185569
title compound
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cc(OCC2CC2)c(C(=O)[NH+]([O-])C2CN3CCC2CC3)cc1Cl
Reaction #2195126
N-(1-azabicyclo[2.2.2]oct-3-yl)-2-cyclopropylmethoxy-4-acetamido-5-chlorobenzamide N-oxide
DOI: 10.6084/m9.figshare.5104873.v1
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