作者:C. Fouquey、J. Jacques、L. Angiolini、M. Tramontini                                    
                                    
                                        DOI:10.1016/s0040-4020(01)97449-6
                                    
                                    
                                        日期:1974.1
                                    
                                    The stereochemical course of the reaction between organo-metals and β-asymmetric amino-ketones has been investigated by varying the nature of the reagent and the substituents in the substrate, as well as the distance of the amino-group from the reaction center.
                                    通过改变试剂和底物中取代基的性质以及
氨基到反应中心的距离,研究了有机
金属与β-不对称
氨基酮之间反应的立体
化学过程。