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CCC(CN1CC2CCC(C1)O2)N1C(=O)C(C)(CC(=O)O)CC(c2cccc(Cl)c2)C1c1ccc(Cl)cc1
Reaction #284027
DOI: 10.1039/C8SC04228D
CC[C@@H](CN1CCOCC1)N1C(=O)[C@@](C)(CC=O)C[C@H](c2cccc(Cl)c2)[C@H]1c1ccc(Cl)cc1
Reaction #1019179
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](CN1CCOCC1)N1C(=O)[C@@](C)(CC(=O)O)C[C@H](c2cccc(Cl)c2)[C@H]1c1ccc(Cl)cc1
Reaction #1019180
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](CN1CCOCC1C)N1C(=O)[C@@](C)(CC(=O)O)C[C@H](c2cccc(Cl)c2)[C@H]1c1ccc(Cl)cc1
Reaction #1019340
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](CN1CC2CCC(C1)O2)N1C(=O)[C@@](C)(CC(=O)O)C[C@H](c2cccc(Cl)c2)[C@H]1c1ccc(Cl)cc1
Reaction #1019342
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](CN1CCOCC1(C)C)N1C(=O)[C@@](C)(CC(=O)O)C[C@H](c2cccc(Cl)c2)[C@H]1c1ccc(Cl)cc1
Reaction #1019343
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC(CN1CCOCC1(C)C)N1C(=O)C(C)(CC(=O)O)CC(c2cccc(Cl)c2)C1c1ccc(Cl)cc1
Reaction #1040756
DOI: 10.1039/C8SC04228D
CC[C@@H](CN1CCOCC1)N1C(=O)[C@@](C)(CC=O)C[C@H](c2cccc(Cl)c2)[C@H]1c1ccc(Cl)cc1
Reaction #1135491
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](CN1CCOCC1C)N1C(=O)[C@@](C)(CC(=O)O)C[C@H](c2cccc(Cl)c2)[C@H]1c1ccc(Cl)cc1
Reaction #1135654
2-((3R,5R,6S)-5-(3-chlorophenyl)-6-(4-chlorophenyl)-3-methyl-1-((2S)-1-(3-methylmorpholino)butan-2-yl)-2-oxopiperidin-3-yl)acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](CN1CC2CCC(C1)O2)N1C(=O)[C@@](C)(CC(=O)O)C[C@H](c2cccc(Cl)c2)[C@H]1c1ccc(Cl)cc1
Reaction #1135656
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](CN1CCOCC1(C)C)N1C(=O)[C@@](C)(CC(=O)O)C[C@H](c2cccc(Cl)c2)[C@H]1c1ccc(Cl)cc1
Reaction #1135657
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC(CN1CCOCC1)N1C(=O)C(C)(CC=O)CC(c2cccc(Cl)c2)C1c1ccc(Cl)cc1
Reaction #1643721
DOI: 10.1039/C8SC04228D
CCC(CN1CCOCC1C)N1C(=O)C(C)(CC(=O)O)CC(c2cccc(Cl)c2)C1c1ccc(Cl)cc1
Reaction #2435040
DOI: 10.1039/C8SC04228D