Ähnlichkeitssuche

329809

CC(C)CCC(COC(F)F)N1CCC(CC(=O)O)CC1c1ccc(C(F)(F)F)cc1
Reaction #190445
DOI: 10.1039/C8SC04228D
CC(C)CCC(c1ccc(I)cc1)N1CCC(CC(=O)O)CC1c1ccc(C(F)(F)F)cc1
Reaction #1021796
DOI: 10.1039/C8SC04228D
CC(C)CCC(c1ccc(C(=O)c2ccccc2)cc1)N1CCC(CC(=O)O)CC1c1ccc(C(F)(F)F)cc1
Reaction #1023541
DOI: 10.1039/C8SC04228D
CC(C)C=CC(CCC(C)C)N1CCC(CC(=O)O)CC1c1ccc(C(F)(F)F)cc1
Reaction #1221164
DOI: 10.1039/C8SC04228D
CC(C)CCC(CC1CCOCC1)N1CCC(CC(=O)O)CC1c1ccc(C(F)(F)F)cc1
Reaction #1224341
DOI: 10.1039/C8SC04228D
C=C(C)C#C[C@H](c1ccc(C(F)(F)F)nc1)N1CC[C@@H](CC(=O)O)C[C@H]1c1ccc(C(F)(F)F)cc1
Reaction #1602540
acid
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C[C@@H]1CCN([C@H](CCC(C)C)CC2CCOCC2)[C@H](c2ccc(C(F)(F)F)cc2)C1
Reaction #1602541
alkane
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC[C@H](CC1CCOCC1)N1CC[C@@H](CC(=O)O)C[C@H]1c1ccc(C(F)(F)F)cc1
Reaction #1602542
acid
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C#C[C@@H](c1ccccc1)N1CC[C@H](CC(=O)O)C[C@@H]1c1ccc(C(F)(F)F)cc1
Reaction #1956940
title compound
Ausbeute 9.5%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C#C[C@H](c1ccc(C(F)(F)C(F)(F)F)cc1)N1CC[C@@H](CC(=O)O)C[C@H]1c1ccc(C(F)(F)F)cc1
Reaction #1956942
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC[C@H](c1ccc(I)cc1)N1CC[C@@H](CC(=O)O)C[C@H]1c1ccc(C(F)(F)F)cc1
Reaction #1956943
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC[C@H](c1ccc(C(=O)c2ccccc2)cc1)N1CC[C@@H](CC(=O)O)C[C@H]1c1ccc(C(F)(F)F)cc1
Reaction #1956944
acid
Ausbeute 53.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC[C@H](c1ccc(Cl)cc1)N1CC[C@@H](CC(=O)O)C[C@H]1c1ccc(C(F)(F)F)cc1
Reaction #1956955
{(2S,4R)-1-[(1R)-1-(4-chlorophenyl)-4-methylpentyl]-2-[4-(trifluoromethyl)phenyl]piperidin-4-yl}acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C#C[C@H](CCC(C)C)N1CC[C@@H](CC(=O)OC)C[C@H]1c1ccc(C(F)(F)F)cc1
Reaction #2029474
alkyne
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)C#C[C@H](CCC(C)C)N1CC[C@@H](CC(=O)O)C[C@H]1c1ccc(C(F)(F)F)cc1
Reaction #2029475
acid
Ausbeute 93.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C[C@@H]1CCN(C(CCC(C)C)CCC(C)C)[C@H](c2ccc(C(F)(F)F)cc2)C1
Reaction #2029476
alkane
Ausbeute 72.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC(CCC(C)C)N1CC[C@@H](CC(=O)O)C[C@H]1c1ccc(C(F)(F)F)cc1
Reaction #2029477
acid
Ausbeute 97.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)/C=C\[C@H](CCC(C)C)N1CC[C@@H](CC(=O)O)C[C@H]1c1ccc(C(F)(F)F)cc1
Reaction #2029478
acid
Ausbeute 85.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC[C@H](CO)N1CC[C@@H](CC(=O)O)C[C@H]1c1ccc(C(F)(F)F)cc1
Reaction #2029479
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC[C@H](COC(C)C)N1CC[C@@H](CC(=O)O)C[C@H]1c1ccc(C(F)(F)F)cc1
Reaction #2029480
title compound
Ausbeute 13.5%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter