85375-47-9Relevant articles and documents
The absolute configuration of the (+)- and (-)-cis- and (+)- and (-)-trans-1-benzyl-4-hydroxypiperidine-3-methanols: An unusual application of the1H-NMR-mosher method
Clerc, Christian,Matarazzo, Igor,Rueedi, Peter
experimental part, p. 14 - 28 (2009/05/30)
The enantiomerically pure title compounds were prepared and the absolute configurations assigned by the high-field 1H-NMR application of the Mosher method on the bis-MTPA derivatives (MTPA - a-methoxy-a-(trifluoromethyl) benzeneacetic acid). Th
Orally Active and Potent Inhibitors of γ-Aminobutyric Acid Uptake
Ali, Fadia E.,Bondinell, William E.,Dandridge, Penelope A.,Frazee, James S.,Garvey, Eleanor,et al.
, p. 653 - 660 (2007/10/02)
3-Pyrrolidineacetic acid (1a), certain piperidinecarboxylic acids - i.e., piperidinecarboxylic acid (2a), 1,2,5,6-tetrahydro-3-pyridinecarboxylic acid (3a), and cis-4-hydroxy-3-piperidinecarboxylic acid (4a) - cis-3-aminocyclohexanecarboxylic acid (5a, ci