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Convergent Synthesis of Trisubstituted Z-Allylic Esters by Wittig-Schlosser Reaction

  作者 HODGSON DAVID M; ARIF TANZEEL  
  选自 期刊  Organic Letters;  卷期  2010年12-18;  页码  4204-4207  
  关联知识点  
 

[摘要]beta-Lithiooxyphosphonium ylides, generated in situ from aldehydes and Wittig reagents, react readily with halomethyl esters to form trisubstituted Z-allylic esters. The methodology was applied to a total synthesis of the geranylgeraniol-derived diterpene (6S,7R,Z)-7-hydroxy-2-((E)-6-hydroxy4-methylhex-4-enylidene)-6,10-dimet hylundec-9-enyl acetate (12).

 
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