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A Three-Step Route to a Tricyclic Steroid Precursor.

  作者 Taber, Douglass F.;Sheth, Ritesh B.;  
  选自 期刊  Journal of Organic Chemistry;  卷期  2008年73-20;  页码  8030-8032  
  关联知识点  
 

[摘要]2-Alkyl cyclohexenones are useful intermediates for org. synthesis. The Wittig reaction of a series of aldehydes with (cyclopropylmethyl)triphenylphosphonium bromide delivered the corresponding alkenyl cyclopropanes. UV irradn. in the presence of Fe(CO)5 converted the alkenyl cyclopropanes to the 2-substituted cyclohexenones. This approach enabled a three-step synthesis of the tricyclic core I of estrone Me ether.

 
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