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64484

Cc1ccc2cccc(N(Cc3c(Cl)ccc([N+](=O)[O-])c3Cl)C(=O)OC(C)(C)C)c2n1
Reaction #272132
DOI: 10.1039/C8SC04228D
CC(=O)NC1CCCc2ccc(C)nc21
Reaction #358990
N-(2-methyl-5,6,7,8-tetrahydroquinolin-8-yl)acetamide
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1nc(C)ccc1N
Reaction #399376
DOI: 10.1039/C8SC04228D
Cc1ccc2cccc(N(Cc3c(Cl)ccc([N+](=O)[O-])c3Cl)C(=O)OC(C)(C)C)c2n1
Reaction #652137
8-[N-tert-butoxycarbonyl-N-(2,6-dichloro-3-nitrobenzyl)amino]-2-methylquinoline
Ausbeute 76.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2cccc(N(Cc3c(Cl)ccc([N+](=O)[O-])c3Cl)C(=O)OC(C)(C)C)c2n1
Reaction #668978
8-[N-tert-butoxycarbonyl-N-(2,6-dichloro-3-nitrobenzyl)amino]-2-methylquinoline
Ausbeute 76.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC1CCCc2ccc(C)nc21
Reaction #807915
N-(2-methyl-5,6,7,8-tetrahydroquinolin-8-yl)acetamide
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2cccc(N(Cc3c(Cl)ccc([N+](=O)[O-])c3Cl)C(=O)OC(C)(C)C)c2n1
Reaction #813508
8-[N-tert-butoxycarbonyl-N-(2,6-dichloro-3-nitrobenzyl)amino]-2-methylquinoline
Ausbeute 76.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(NC(=O)OC(C)(C)C)c(C(=O)Nc2ccnc(Cl)c2)n1
Reaction #925405
DOI: 10.1039/C8SC04228D
Cc1ccc2cccc(N(Cc3c(Cl)ccc([N+](=O)[O-])c3Cl)C(=O)OC(C)(C)C)c2n1
Reaction #951785
8-[N-tert-butoxycarbonyl-N-(2,6-dichloro-3-nitrobenzyl)amino]-2-methylquinoline
Ausbeute 76.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC1CCCc2ccc(C)nc21
Reaction #986854
product
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC1CCCc2ccc(C)nc21
Reaction #987002
product
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1nc(C)ccc1NC(=O)OC(C)(C)C
Reaction #1181952
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1nc(C)ccc1N
Reaction #1181953
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC1CCCc2ccc(C)nc21
Reaction #1711500
product
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2cccc(NC(=O)C(C)(C)O)c2n1
Reaction #1723707
product
Ausbeute 67.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1nc(C)ccc1NC(=O)OC(C)(C)C
Reaction #2306651
title compound
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(NC(=O)OC(C)(C)C)c(C(=O)Nc2ccnc(Cl)c2)n1
Reaction #2306652
title compound
Ausbeute 73.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC1CCCc2ccc(C)nc21
Reaction #2504372
N-(2-methyl-5,6,7,8-tetrahydroquinolin-8-yl)acetamide
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1