dopamine

CN1CCC[C@H]1c1cccnc1
Reaction #1858
(S)-(-)-nicotine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN1CCC[C@H]1c1cccnc1
Reaction #2817
(S)-(-)-nicotine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN1CCC[C@H]1c1cccnc1
Reaction #5022
(S)-(-)-nicotine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CN1CCC[C@H]1c1cccnc1
Reaction #6467
(S)-(-)-nicotine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Cl.Clc1ccc(C23CNCC2C3)cc1Cl
Reaction #11492
(−)-1-(3,4-Dichlorophenyl)-3-azabicyclo[3.1.0]hexane HCl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CS(=O)(=O)N(CCCN)Cc1cccc(-c2ccnc(NCCc3ccc(O)c(O)c3)n2)c1
Reaction #42984
N-(3-Amino-propyl)-N-(3-{2-[2-(3,4-dihydroxy-phenyl)-ethylamino]-pyrimidin-4-yl}-benzyl)-methanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN1CCC[C@H]1c1cccnc1
Reaction #80685
(S)-(-)-nicotine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Oc1cc2c(cc1O)C(CN(c1ccccc1)c1ccccc1)NCC2
Reaction #190736
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NS(=O)(=O)c1ccc(OCC2NCCc3cc(O)c(O)cc32)cc1
Reaction #245265
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cl
Reaction #246591
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CN1CCC[C@H]1c1cccnc1
Reaction #322444
(S)-(-)-nicotine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
CN1CCC[C@H]1c1cccnc1
Reaction #336467
(S)-(-)-nicotine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
O=C(OCc1ccccc1)N(CC1NCCc2cc(O)c(O)cc21)c1cccc(F)c1
Reaction #379086
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(C)(C)C(=O)NCCc1ccc(O)c(O)c1
Reaction #381469
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CN1CCC[C@H]1c1cccnc1
Reaction #482013
(S)-(−)-nicotine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
CN1CCC[C@H]1c1cccnc1
Reaction #486949
(S)-(-)-nicotine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_10
Cl.Clc1ccc(C23CNCC2C3)cc1Cl
Reaction #500956
(−)-1-(3,4-Dichlorophenyl)-3-azabicyclo[3.1.0]hexane HCl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
CN1CC[C@]23c4c5ccc(O)c4O[C@H]2[C@@H](O)C=C[C@H]3[C@H]1C5
Reaction #534889
morphine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
COc1cc(/C=C/C(=O)NCCc2ccc(O)c(O)c2)ccc1O
Reaction #535366
N-trans-feruloyldopamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
N[C@@H](Cc1ccc(O)c(O)c1)C(=O)O
Reaction #539521
levodopa
Ausbeute 458.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
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