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首页> 外文期刊>Bulletin of the Korean Chemical Society >Regioselectivities in Fe(III)‐catalyzed Cycloisomerization Reactions of γ‐Allenyl Alcohols
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Regioselectivities in Fe(III)‐catalyzed Cycloisomerization Reactions of γ‐Allenyl Alcohols

机译:Fe(III)催化的γ-烯丙基醇环化反应中的区域选择性

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Irona??catalyzed intramolecular hydroalkoxylation reactions of allenes were performed to provide various tetrahydrofurans by regioselective 5a??exo cyclization pathway, as the Lewis acidic activation of Fe(III) salts toward unsaturated C?£?C bonds, allenes and alkenes. Cyclohexyl substituted allenes especially isomerized to dienes at a rapid rate, which underwent a competing 6a??endo cyclization mode. The plausible mechanism was presented by experimental results of the reaction intermediates and computational study of Fea??allene and Fea??diene complexes.
机译:进行了艾伦烯的铁氧催化的分子内加氢烷氧基化反应,通过区域选择性的5a-exo环化途径提供了各种四氢呋喃,这是因为Fe(III)盐向不饱和C 3 -C碳键,艾伦和烯烃的路易斯酸性活化。环己基取代的异烯特别是迅速地异构化成二烯,这经历了竞争性的6α-β-内酯环化模式。通过反应中间体的实验结果以及Fea ?? Allene和Fea ?? diene配合物的计算研究,提出了可能的机理。

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