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34503

c1ccc(CCN2CCCc3ccccc32)cc1
Reaction #202144
DOI: 10.1039/C8SC04228D
COc1cc(CC(=O)N2CCCc3cc(CC(NC(C)=O)C(=O)O)ccc32)ccc1NC(=O)Nc1ccccc1C
Reaction #302661
DOI: 10.1039/C8SC04228D
O=C(NCC1CCc2ccccc2N1CCc1ccccc1)Nc1cccc2[nH]ncc12
Reaction #386063
DOI: 10.1039/C8SC04228D
CC1(C)CCc2ccccc2N1CC(=O)c1ccc(F)cc1
Reaction #460763
N-(4-fluorobenzoylmethyl)-2,2-dimethyl-1,2,3,4-tetrahydroquinoline
Ausbeute 85.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CC(=O)N2CCCc3cc(CCC(=O)O)ccc32)ccc1NC(=O)Nc1ccccc1C
Reaction #483890
title compound
Ausbeute 65.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1NC(=O)Nc1ccc(CC(=O)N2c3ccccc3CCC2C2CCOC(=O)C2)cc1
Reaction #483894
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CC(=O)N2CCCc3cc(CC(NC(C)=O)C(=O)O)ccc32)ccc1NC(=O)Nc1ccccc1C
Reaction #483895
title compound
Ausbeute 9.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCc1ccc2c(c1)CCCN2C(=O)Cc1ccc(NC(=O)Nc2ccccc2C)c(OC)c1
Reaction #483896
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #736379
hydrochloride salt
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCc1ccc2c(c1)CCCN2C(=O)Cc1ccc(NC(=O)Nc2ccccc2C)c(OC)c1
Reaction #901544
DOI: 10.1039/C8SC04228D
CC1(C)CN(C(=O)Cc2ccccc2)c2ccccc2C1n1cncc1CO
Reaction #1184970
crude compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCC1CCc2ccccc2N1CCc1ccccc1)Nc1cccc2[nH]ncc12
Reaction #1245998
title compound
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCCN1CCOc2ccc(COC3CN(C(=O)OCc4ccccc4)CCC3c3ccc(CC(=O)N4CCCc5ccccc54)cc3)cc21
Reaction #1263788
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)n1ncc2c(NC(=O)NCC3CCc4ccccc4N3CCc3ccccc3)cccc21
Reaction #1323142
DOI: 10.1039/C8SC04228D
C[C@H](NC(=O)OC(C)(C)C)C(=O)NC1C(=O)N2CCCc3cccc(c32)-c2ccccc21
Reaction #1354361
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COCCCN1CCOc2ccc(COC3CN(C(=O)OCc4ccccc4)CCC3c3ccc(CC(=O)N4CCCc5ccccc54)cc3)cc21
Reaction #1634523
DOI: 10.1039/C8SC04228D
C[C@H](NC(=O)OC(C)(C)C)C(=O)NC1C(=O)N2CCCc3cccc(c32)-c2ccccc21
Reaction #1847282
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1ccc2c(c1)C(C)(C)CC(=O)N2CCc1ccccc1
Reaction #1928059
oil
Ausbeute 34.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)n1ncc2c(NC(=O)NCC3CCc4ccccc4N3CCc3ccccc3)cccc21
Reaction #2179362
titled compound
Ausbeute 79.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCC1CCc2ccccc2N1CCc1ccccc1)Nc1cccc2[nH]ncc12
Reaction #2179363
title compound
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
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