作者:Katsukiyo Miura、Mizuki Takasumi、Takeshi Hondo、Hiroshi Saito、Akira Hosomi                                    
                                    
                                        DOI:10.1016/s0040-4039(97)00981-7
                                    
                                    
                                        日期:1997.6
                                    
                                    In the presence of TiCl4, methylenecyclopropane (1a) easily reacted with aliphatic aldehydes to give the β-(chloromethyl)allylated products 2 in good yields along with a small amount of the methylenetetrahydrofurans 3. The reaction with chiral α- and β-alkoxy aldehydes proceeded with high levels of chelation control.
                                    在TiCl 4的存在下,
亚甲基环丙烷(1a)容易与脂族醛反应,以高收率得到β-(
氯甲基)烯丙基化产物2以及少量的亚甲基
四氢呋喃3。与手性α-和β-烷氧基醛的反应以高
水平的螯合控制进行。