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首页> 外文期刊>Advanced synthesis & catalysis >Triethylamine Enables Catalytic Generation of Oxidopyrylium Ylides for [5+2] Cycloadditions with Alkenes: An Efficient Entry to 8-Oxabicyclo[3.2.1]octane Frameworks
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Triethylamine Enables Catalytic Generation of Oxidopyrylium Ylides for [5+2] Cycloadditions with Alkenes: An Efficient Entry to 8-Oxabicyclo[3.2.1]octane Frameworks

机译:三乙胺能够用烯烃催化产生氧化钇yliders [5 + 2]环加入的氧化烯烃:高效进入8-氧基阳岩[3.2.1]辛烷值框架

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摘要

An efficient method for the preparation of a range of 8-oxabicyclo[3.2.1]octane derivatives including synthetic intermediates of natural products is described, in which triethylamine effectively catalyzes [5+2] cycloaddition reactions between oxidopyrylium ylides and alkenes. This method can be applied not only to intermolecular cycloadditions with various alkenes but also to intramolecular cycloadditions. The key finding is that the combined use of organic bases having appropriate basicity and oxidopyrylium ylide precursors bearing a suitable leaving group facilitates the base-assisted generation of oxidopyrylium ylides in a catalytic manner.
机译:制备包括天然产物的合成中间体的8-oxabidicClO [3.2.1]辛烷值的高效方法,其中三乙胺有效地催化氧化镍杯和烯烃之间的[5 + 2]环加成反应。 该方法不仅可以应用于各种烯烃的分子环加成,而且还可以应用于分子加速。 关键发现是具有含有合适的离去基团的适当碱性和氧化甘油钇前体的有机碱的结合使用促进了催化方式的基础辅助氧化钇。

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