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Heterogeneous diastereoselective hydrogenation of pyridine and corresponding enamine covalently bound to pantolactone
Authors:Najiba Douja, Raluca Malacea, Mich  le Besson,Catherine Pinel
Affiliation:

Institut de Recherches sur la Catalyse-CNRS, 2 Avenue Albert Einstein, 69626, Villeurbanne Cedex, France

Abstract:The diastereoselective hydrogenation of 2-methyl nicotinic acid covalently bound to pantolactone was studied over supported metallic catalysts. With this chiral auxiliary, a two-steps reaction was observed with formation of tetrahydropyridine intermediate. The influence of different reaction parameters on the diastereoselectivity of the hydrogenation of pyridine and enamine substrates was studied.
Keywords:Hydrogenation   Pyridine   Pantolactone   Nicotinic
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