名称:
                                Bromation des enamines du prénal et du crotonaldéhyde. Voie d'accès aux ω-bromo aldéhydes et ω-bromo acétals correspondants.
                             
                            
                                摘要:
                                Bromination of enamines of prenal and crotonaldehyde yields the corresponding omega-bromoaldehydes via the simple hydrolysis of iminium salts. The carbonyl function of these aldehydes can be protected as acetals or dioxolane. The overall process can be realized in a one pot procedure. The dioxolane is the starting material of a phosphonate which allows by condensation with beta-ionylidenacetaldehyde a direct access to the retinal with a 27.5% overall yield from the enamine 2
                             
                                                            
                                    DOI:
                                    10.1016/s0040-4039(00)61186-3