Michael Addition Reactions of the Highly Functionalized Zinc-Copper Reagents RCu(CN)ZnI to (Tropone)iron Tricarbonyl Promoted by Boron Trifluoride Etherate

Ming Chang P. Yeh*, Chong Chen Hwu, Chuen Her Ueng, Huei Lin Lue

*此作品的通信作者

研究成果: 雜誌貢獻期刊論文同行評審

11 引文 斯高帕斯(Scopus)

摘要

The zinc-copper reagents RCu(CN)ZnI, containing various functional groups such as a cyanide, ester, thio ester or benzyl, react with (tropone)iron tricarbonyl in the presence of an excess of boron trifluoride etherate to afford the Michael adducts in excellent yields. Cyano-substituted 1.4-adducts undergo an intramolecular cyclization reaction in situ, leading to highly functionalized bicyclo[5.3.0]decane and-[5.4.0]undecane derivatives, whereas treatments of an ester-substituted 1.4-adduct with lithium diisopropylamide (LDA) under an atmosphere of carbon monoxide furnishs a highly functionalized bridged bicyclo[4.2.1] nonenecarboxylic acid derivative in 88 % yield.

原文英語
頁(從 - 到)1788-1794
頁數7
期刊Organometallics
13
發行號5
DOIs
出版狀態已發佈 - 1994 五月 1

ASJC Scopus subject areas

  • 物理與理論化學
  • 有機化學
  • 無機化學

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