2-(2-oxo-3,3-diphenylpiperidin-1-yl)acetic acid

O=C(CN1CCCC(c2ccccc2)(c2ccccc2)C1=O)N1CCC(=C(c2ccc(F)cc2)c2ccc(F)cc2)CC1
Reaction #173683
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(CN1CCCC(c2ccccc2)(c2ccccc2)C1=O)N1CCC(C(O)(c2ccccc2)c2ccccc2)CC1
Reaction #183727
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(CN1CCCC(c2ccccc2)(c2ccccc2)C1=O)N1CCN(C(=O)OCc2ccccc2)CC1
Reaction #246814
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(CN1CCCC(c2ccccc2)(c2ccccc2)C1=O)N1CCN(Cc2cccc(C(F)(F)F)c2)CC1
Reaction #259594
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(CN1CCCC(c2ccccc2)(c2ccccc2)C1=O)NC1CCOc2ccc(F)cc21
Reaction #281134
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(CN1CCCC(c2ccccc2)(c2ccccc2)C1=O)N1CCN(C(c2ccc(F)cc2)c2ccc(F)cc2)CC1
Reaction #284757
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(CN1CCCC(c2ccccc2)(c2ccccc2)C1=O)N1CCN(Cc2ccc(Cl)cc2Cl)CC1
Reaction #385709
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(CN1CCCC(c2ccccc2)(c2ccccc2)C1=O)N1CCN(Cc2ccc(C(F)(F)F)cc2)CC1
Reaction #388253
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(CN1CCCC(c2ccccc2)(c2ccccc2)C1=O)N1CCC(C(c2ccccc2)c2ccccc2)CC1
Reaction #394699
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(CN1CCCC(c2ccccc2)(c2ccccc2)C1=O)N1CCCC1c1ccc(F)cc1
Reaction #892384
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
O=C(O)CN1CCCC(c2ccccc2)(c2ccccc2)C1=O
Reaction #909234
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
O=C(CN1CCCC(c2ccccc2)(c2ccccc2)C1=O)N1CCCCC1c1ccc(F)cc1
Reaction #911938
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
O=C(CN1CCCC(c2ccccc2)(c2ccccc2)C1=O)N1CCOC(c2ccccc2)C1
Reaction #1021742
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
O=C(CN1CCCC(c2ccccc2)(c2ccccc2)C1=O)N1CCC(c2ccccc2)(c2ccccc2)CC1
Reaction #1038092
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
CC(CNC(=O)CN1CCCC(c2ccccc2)(c2ccccc2)C1=O)(c1ccccc1)c1ccccc1
Reaction #1047513
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
O=C(CN1CCCC(c2ccccc2)(c2ccccc2)C1=O)NC1CCN(C(c2ccccc2)c2ccccc2)CC1
Reaction #1201075
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
O=C(CN1CCCC(c2ccccc2)(c2ccccc2)C1=O)N1CCC(Oc2ccc(Cl)cc2)CC1
Reaction #1216100
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
CC1(NC(=O)CN2CCCC(c3ccccc3)(c3ccccc3)C2=O)CCN(Cc2ccccc2)C1
Reaction #1231839
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
O=C(CN1CCCC(c2ccccc2)(c2ccccc2)C1=O)N1CCC(c2ccc(F)cc2)(c2ccc(F)cc2)C1
Reaction #1318504
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
CC(C)(C)OC(=O)NC1CCN(C(=O)CN2CCCC(c3ccccc3)(c3ccccc3)C2=O)CC1
Reaction #1645269
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
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