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OCCCCCc1cccc(Br)c1

C[C@H]1[C@H](OCC(C)(C)C)OC[C@H]([C@@H](O)[C@@H](N)Cc2cc(F)cc(Br)c2)N1C(=O)OC(C)(C)C
Reaction #48738
title compound
Ausbeute 99.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1cc(F)cc(C[C@H](NC(C)=O)[C@H](O)[C@H]2CO[C@@H](OCC(C)(C)C)[C@H](C)N2C(=O)OC(C)(C)C)c1
Reaction #48739
title compound
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H](Cc1cc(F)cc(CCC(C)C)c1)[C@H](O)[C@H]1CO[C@@H](OCC(C)(C)C)[C@H](C)N1C(=O)OC(C)(C)C
Reaction #48740
title compound
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccccc1-c1cc(F)cc(C[C@H](NC(C)=O)[C@H](O)[C@H]2CO[C@@H](OCC(C)(C)C)[C@H](C)N2C(=O)OC(C)(C)C)c1
Reaction #48741
title compound
Ausbeute 46.4%DOI: 10.6084/m9.figshare.5104873.v1
OCCCCCc1cccc(Br)c1
Reaction #58858
5-(3-bromophenyl)pentan-1-ol
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
FCCCCCc1cccc(Br)c1
Reaction #58859
1-bromo-3-(5-fluoropentyl)benzene
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC1CCc2cc(Br)ccc2N1
Reaction #80760
crude compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC1CCc2cc(Br)cc3[nH]c(=O)c(=O)n1c23
Reaction #80762
title compound
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC1CCc2cc(Br)cc3[nH]c(=O)c(=O)n1c23)NCc1ccccc1
Reaction #80776
title compound
Ausbeute 90.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC1CCc2cc(Br)cc3[nH]c(=O)c(=O)n1c23)NCCc1ccccc1
Reaction #80777
title compound
Ausbeute 87.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC1CCc2cc(Br)cc3[nH]c(=O)c(=O)n1c23)NC1CC1
Reaction #80778
title compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cccc(NC(=O)CC2CCc3cc(Br)cc4[nH]c(=O)c(=O)n2c34)c1
Reaction #80779
title compound
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(NC(=O)CC2CCc3cc(Br)cc4[nH]c(=O)c(=O)n2c34)cc1
Reaction #80780
title compound
Ausbeute 47.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccccc1NC(=O)CC1CCc2cc(Br)cc3[nH]c(=O)c(=O)n1c23
Reaction #80781
title compound
Ausbeute 59.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC1CCc2cc(Br)cc3[nH]c(=O)c(=O)n1c23)NC1CCCCC1
Reaction #80782
title compound
Ausbeute 86.1%DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1ccccc1NC(=O)CC1CCc2cc(Br)cc3[nH]c(=O)c(=O)n1c23
Reaction #80783
title compound
Ausbeute 17.2%DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1cccc(NC(=O)CC2CCc3cc(Br)cc4[nH]c(=O)c(=O)n2c34)c1
Reaction #80784
title compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1ccc(NC(=O)CC2CCc3cc(Br)cc4[nH]c(=O)c(=O)n2c34)cc1
Reaction #80785
title compound
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1NC(=O)CC1CCc2cc(Br)cc3[nH]c(=O)c(=O)n1c23
Reaction #80786
title compound
Ausbeute 86.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(NC(=O)CC2CCc3cc(Br)cc4[nH]c(=O)c(=O)n2c34)c1
Reaction #80787
title compound
Ausbeute 96.8%DOI: 10.6084/m9.figshare.5104873.v1
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