Enantioselective hydrogenation of N-acetyl dehydrophenylalanine methyl ester using cinchonine-modified Pd/Al₂O₃ catalysts

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• 作者：Nicola J. Coulston ; Edward L. Jeffery ; Richard P.K. Wells ; Paul McMorn ; Peter B. Wells ; David J. Willock and Graham J. Hutchings
• 关键词：Hydrogenation ; Heterogeneous ; Enantioselective ; Computer modeling ; Cinchonine
• 刊名：Journal of Catalysis
• 出版年：2006
• 出版时间：25 October 2006
• 年：2006
• 卷：243
• 期：2
• 页码：360-367
• 全文大小：224 K

文摘

The enantioselective hydrogenation of (E)-N-acetyl dehydrophenylalanine methyl ester (NADPME) to N-acetyl phenylalanine methyl ester was investigated using cinchonine-modified Pd/Al₂O₃ catalysts. The catalysts were evaluated for this reaction using methanol as solvent with various cinchonine:NADPME molar ratios. Enantioselectivity was sensitive to this ratio as well as to the solvent, and in general, ee increased with the polarity of the solvent. The highest ee of 33 % was observed with DMF/water as solvent, but attempts to improve upon this have been unsuccessful. We used combined structural modification of the reactant and alkaloid together with computer simulations to gain insight into why the low enantioselectivity persists. Using this approach, we propose a model in which NADPME interacts as a monomer with cinchonine via hydrogen bonding between the protonated quinuclidine-N of cinchonine and the hydrogen bond acceptor functional groups of NADPME, which induces enantioselection. DFT level calculations of these interactions show that NHOC hydrogen bonding gives the most stable complexes and that the lowest pro-S and pro-R dimer forms are practically isoenergetic, although higher energy dimer pairs show discrimination, thereby helping to explain the disappointing ee obtained to date.