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        Synthesis  2011(15): 2478-2482  
DOI: 10.1055/s-0030-1260117
   DOI: 10.1055/s-0030-1260117
PAPER
© Georg Thieme Verlag
      Stuttgart ˙ New YorkN-tert-Butanesulfinyl Imines in Alkaloid Synthesis: Stereoselective Synthesis of (R)-Coniine and Formal Synthesis of (S)-δ-Coniceine [¹]
Further Information
            
               
                  
                        
                              Received
                              14 April 2011 
                      
Publication Date:
14 July 2011 (online)
            
         
      
   Publication History
Publication Date:
14 July 2011 (online)

Abstract
A stereoselective synthesis of the hemlock alkaloid (R)-coniine and a formal synthesis of the indolizidine alkaloid (S)-δ-coniceine were achieved by means of a highly diastereoselective Barbier-type indium-mediated allylation strategy involving (S)-(N-tert-butanesulfinyl)imines.
Key words
alkaloids - stereoselective synthesis - piperidines
- Supporting Information for this article is available online:
               
               
- Supporting Information (PDF)
Part 49 in the series ‘Synthetic Studies on Natural Products’.
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Part 49 in the series ‘Synthetic Studies on Natural Products’.
 
    