Ähnlichkeitssuche

391936

CC(C)CC(NC(=O)N1CCCCCC1)C(=O)NC(COC(C)(C)C)Cc1ccc(OCc2ccccc2)cc1
Reaction #366059
white solid
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C[C@@H](N)Cc1ccc(OCc2ccccc2)cc1
Reaction #366071
(S)-3-(4-benzyloxy-phenyl)-N1,N1-diethyl-propane-1,2-diamine
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C[C@H](Cc1ccc(OCc2ccccc2)cc1)NC(=O)[C@H](CC(C)C)NC(=O)N1CCCCCC1
Reaction #366072
title compound
Ausbeute 19.2%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C[C@@H](N)Cc1ccc(OCc2ccccc2)cc1
Reaction #516314
(S)-3-(4-benzyloxy-phenyl)-N1,N1-diethyl-propane-1,2-diamine
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(C)C(NC(=O)N1CCCCCC1)C(=O)NC(Cc1ccc(OCc2ccccc2)cc1)C(=O)OC(C)(C)C
Reaction #902789
DOI: 10.1039/C8SC04228D
CC(C)CC(NC(=O)N1CCCCCC1)C(=O)NC(Cc1ccc(OCc2ccccc2)cc1)C(=O)OC(C)(C)C
Reaction #1046747
DOI: 10.1039/C8SC04228D
CC(Cc1ccc(OCc2ccccc2)cc1)NCC=C(c1ccccc1)c1ccccc1
Reaction #1152656
1-(p-benzyloxyphenyl)-2-(3,3-diphenylallylamino)-propane
DOI: 10.6084/m9.figshare.5104873.v1
CC(Cc1ccc(OCc2ccccc2)cc1)NCCCC(c1ccc(F)cc1)c1ccc(F)cc1.Cl
Reaction #1152658
1-(p-benzyloxyphenyl)-2-[4,4-di-(4-fluorophenyl)-butylamino]-propane hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CC(N)Cc1ccc(OCc2ccccc2)cc1
Reaction #1240534
DOI: 10.1039/C8SC04228D
CC(C)CC(NC1CCOCC1)C(=O)NC(Cc1ccc(OCc2ccccc2)cc1)C(=O)OC(C)(C)C
Reaction #2041097
title compound
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC(NCC1c2ccccc2-c2ccccc21)C(=O)NC(Cc1ccc(OCc2ccccc2)cc1)C(=O)OC(C)(C)C
Reaction #2317468
title compound
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](NC(=O)N1CCCCCC1)C(=O)N[C@H](Cc1ccc(OCc2ccccc2)cc1)C(=O)OC(C)(C)C
Reaction #2317477
title compound
Ausbeute 79.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@@H](NC(=O)N1CCCCCC1)C(=O)N[C@@H](Cc1ccc(OCc2ccccc2)cc1)C(=O)OC(C)(C)C
Reaction #2317478
title compound
Ausbeute 86.1%DOI: 10.6084/m9.figshare.5104873.v1
CCC(C)[C@H](NC(=O)N1CCCCCC1)C(=O)N[C@@H](Cc1ccc(OCc2ccccc2)cc1)C(=O)OC(C)(C)C
Reaction #2317479
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(NC(=O)N1CCCCCC1)C(=O)NC(Cc1ccc(OCc2ccccc2)cc1)C(=O)OC(C)(C)C
Reaction #2317480
title compound
Ausbeute 48.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C(Cc1ccc(OCc2ccccc2)cc1)NC(=O)CNC(=O)N1CCCCCC1
Reaction #2317481
title compound
Ausbeute 46.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC(NC(=O)N1CCN(C)CC1)C(=O)NC(Cc1ccc(OCc2ccccc2)cc1)C(=O)OC(C)(C)C
Reaction #2317482
title compound
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC(NC(=O)N1CCN(c2ccccc2)CC1)C(=O)NC(Cc1ccc(OCc2ccccc2)cc1)C(=O)OC(C)(C)C
Reaction #2317483
title compound
Ausbeute 46.0%DOI: 10.6084/m9.figshare.5104873.v1