Ähnlichkeitssuche

72230

CC1(C)CCC2(CC1)N([C@H](c1ccccc1)[C@@H](O)c1ccccc1)[C@@H](C(=O)N[C@H]1CC[C@H](O)CC1)[C@H](c1cccc(Cl)c1F)C21C(=O)Nc2cc(Cl)ccc21
Reaction #557843
title compound
Ausbeute 101.1%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC2(CC1)N([C@H](c1ccccc1)[C@@H](O)c1ccccc1)[C@@H](C(=O)N[C@H]1CC[C@H](CO)CC1)[C@H](c1cccc(Cl)c1F)C21C(=O)Nc2nc(Cl)ccc21
Reaction #557845
title compound
Ausbeute 83.4%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC2(CC1)N([C@H](c1ccccc1)[C@@H](O)c1ccccc1)[C@@H](C(=O)NCC[C@H](O)CO)[C@H](c1cccc(Cl)c1F)C21C(=O)Nc2cc(Cl)ccc21
Reaction #557846
title compound
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC2(CC1)N[C@@H](C(=O)O)[C@H](c1cccc(Cl)c1F)C21C(=O)Nc2cc(Cl)ccc21
Reaction #557848
title compound
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC2(CC1)N([C@H](c1ccccc1)[C@@H](O)c1ccccc1)[C@@H](C(=O)O)[C@H](c1ccnc(Cl)c1F)C21C(=O)Nc2cc(Cl)ccc21
Reaction #557850
(4′S,5′R)-6″-chloro-4′-(2-chloro-3-fluoropyridin-4-yl)-1′-[(1R,2S)-2-hydroxy-1,2-diphenylethyl]-4,4-dimethyl-2″-oxo-1″,2″-dihydrodispiro[cyclohexane-1,2′-pyrrolidine-3′,3″-indole]-5′-carboxylic acid
Ausbeute 100.4%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC2(CC1)N([C@H](c1ccccc1)[C@@H](O)c1ccccc1)[C@@H](C(=O)N[C@@H]1CC[C@@H](CO)OC1)[C@H](c1ccnc(Cl)c1F)C21C(=O)Nc2cc(Cl)ccc21
Reaction #557852
title compound
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC2(CC1)N[C@@H](C(=O)O)[C@H](c1cccc(Cl)c1F)C21C(=O)Nc2cc(Cl)ncc21
Reaction #557865
title compound
Ausbeute 65.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CC[C@@H](CO)OC1)OCc1ccccc1
Reaction #557872
title compound
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCC2(CC1)N([C@H](c1ccccc1)[C@@H](O)c1ccccc1)[C@@H](C(=O)O)[C@H](c1ccnc(Cl)c1F)C21C(=O)Nc2cc(Cl)ccc21
Reaction #2287509
(4′S,5′R)-6″-chloro-4′-(2-chloro-3-fluoropyridin-4-yl)-1′-[(1R,2S)-2-hydroxy-1,2-diphenylethyl]-4,4-dimethyl-2″-oxo-1″,2″-dihydrodispiro[cyclohexane-1,2′-pyrrolidine-3′,3″-indole]-5′-carboxylic acid
Ausbeute 100.4%DOI: 10.6084/m9.figshare.5104873.v1