作者: G. Neri , L. Mercadante , A. Donato , A. M. Visco , S. Galvagno
DOI: 10.1007/BF00807117
关键词: Double bond 、 Citronellal 、 Ruthenium 、 Citral 、 Chemistry 、 Noyori asymmetric hydrogenation 、 Solvent effects 、 Catalysis 、 Organic chemistry 、 Cyclohexane
摘要: A series of ruthenium supported catalysts were prepared and investigated in the liquid-phase hydrogenation citral. The mechanism reaction was found to be dependent on Ru precursor, support solvent used. On sample from RuCl3 acetals citronellal formed with subsequent isolated C=C double bond. samples obtained precursors which do not contain chloride ions, main product. Hydrogenation bond negligible. Using cyclohexane as solvent, a large amount isopulegol also obtained. results citral have been correlated presence acid sites incompletely reduced favour cyclization formation citronellal. basis reported results, scheme for over is proposed.