1126736-34-2Relevant academic research and scientific papers
Daucus carota mediated-reduction of cyclic 3-oxo-amines
Lacheretz, Romain,Pardo, Domingo Gomez,Cossy, Janine
supporting information; experimental part, p. 1245 - 1248 (2009/08/08)
Carrots (Daucus carota) were used to reduce cyclic amino-ketones in high yields and enantiomeric excesses. This cheap, eco-compatible, and efficient reducing reagent allows the easy access to precursors of biologically active products.
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
