试剂                        
                
                                
                        
                            化学                        
                
                                
                        
                            亚砜                        
                
                                
                        
                            溶剂                        
                
                                
                        
                            二甲基亚砜                        
                
                                
                        
                            组合化学                        
                
                                
                        
                            有机化学                        
                
                        
                    
            作者
            
                Christine M. M. Hendriks,Philip Lamers,Julien Engel,Carsten Bolm            
         
                    
        
    
            
            标识
            
                                    DOI:10.1002/adsc.201300766
                                    
                                
                                 
         
        
                
            摘要
            
            Abstract Sulfoxides can directly be converted into N ‐cyanosulfilimines using a new Burgess‐type reagent. By applying this strategy with a related reagent variant, synthetically valuable N H‐sulfoximines have been prepared from sulfoxides via N ‐protected sulfilimines. The practical three‐step reaction sequence is generally high yielding and applicable to a wide range of substrates. The sulfoxide‐to‐sulfilimine conversion can also be performed under solvent‐reduced conditions in a ball mill. magnified image
         
            
 
                 
                
                    
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