#11206021

CC(C)C(C(=O)Cl)c1ccccc1
Reaction #809893
3-methyl-2-phenylbutyryl chloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_11
CC(C)C(C(=O)N[C@H]1CC[C@H]2CN(Cc3ccccc3)C[C@H]21)c1ccccc1
Reaction #1179654
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
O=C(N[C@@H]1CC[C@@H]2CN(Cc3cccc(C(F)(F)F)c3)C[C@@H]21)C(C1CCCCC1)C1CCCCC1
Reaction #1179719
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
CC(C)C(C(=O)N1C[C@H]2CC[C@H](NC(=O)OC(C)(C)C)[C@H]2C1)c1ccccc1
Reaction #1179744
tert-butyl(3aR,4S,6aS)-2-(3-methyl-2-phenylbutanoyl)octahydrocyclopenta[c]pyrrol-4-ylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
CC(C)C(CO)c1ccccc1
Reaction #1622330
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
CC(C)C(C(=O)NC1CCC2CN(Cc3ccccc3)CC21)c1ccccc1
Reaction #1648934
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
CC(C)C(C(=O)N[C@H]1CC[C@H]2CN(Cc3ccccc3)C[C@H]21)c1ccccc1
Reaction #2450626
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_04
O=C(N[C@@H]1CC[C@@H]2CN(Cc3cccc(C(F)(F)F)c3)C[C@@H]21)C(C1CCCCC1)C1CCCCC1
Reaction #2450694
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_04