作者:Matthias Moens、Matthias D’hooghe、Norbert De Kimpe                                    
                                    
                                        DOI:10.1016/j.tetlet.2013.08.127
                                    
                                    
                                        日期:2013.11
                                    
                                    A three-step synthesis towards 1-aminomethy1-1-fluorocycloalkanes was developed starting from methylenecycloalkanes. Methylenecyclobutane, methylenecyclopentane and methylenecyclohexane were first bromofluorinated to provide the corresponding Markovnikov products, 1-bromomethy1-1-fluorocycloalkanes, which were then converted towards the title compound via azide substitution and hydrogenation. The bromofluorination of methylenecyclopropane, however, led to both the Markovnikov and the anti-Markovnikov product. (C) 2013 Elsevier Ltd. All rights reserved.