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PALLADIUM-CATALYZED TANDEM COUPLING REACTION OF ALKYNE, CONJUGATED DIENE, AND TRIETHYLBORANE

  作者 TAKUSHIMA DAIKI; FUKUSHIMA MASAHIRO; SATOMURA HIDEAKI; ONODERA GEN; KIMURA MASANARI  
  选自 期刊  Heterocycles;  卷期  2012年86-1;  页码  171-180  
  关联知识点  
 

[摘要]Pd(0) catalyst promotes three-component coupling reactions of allylic alcohols and vinylcyclopropanes with terminal alkynes and triethylborane to provide (E)-1-substituted 2-ethyl-1,4-pentadienes and (E)-1-substituted 2-ethyl-1,4-heptadienes involving geminal ethylation and allylation at the acetylenic terminal carbon atom with high regio- and stereoselectivities. 1,3-Butadiene and bis-dienes can act as allylating agents to undergo the multi-component coupling reactions, accompanied by dimerization of the diene moieties, to provide 1,4,9-decatrienes and pyrrolidines with excellent regio- and stereoselectivities.

 
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