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首页> 外文期刊>Molecules >Stereoselective Synthesis of 5-7 membered Cyclic Ethers by Deiodonative Ring-Enlargement Using Hypervalent Iodine Reagents
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Stereoselective Synthesis of 5-7 membered Cyclic Ethers by Deiodonative Ring-Enlargement Using Hypervalent Iodine Reagents

机译:使用高价碘试剂通过去碘环扩大立体选择性合成5-7元环醚

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摘要

Stereoselective synthesis of 5-7 membered cyclic ethers was achieved by deiodonative ring-enlargement of cyclic ethers having an iodoalkyl substituent. The reaction took place readily under mild conditions using hypervalent iodine compounds and an acetoxy or a trifluoroacetoxy group was introduced into the rings depending on the hypervalent iodine reagent employed. The use of hexafluoroisopropanol (HFIP) as solvent is critical.
机译:通过具有碘代烷基取代基的环状醚的去碘环扩环来实现5-7元环状醚的立体选择性合成。反应在温和条件下使用高价碘化合物容易进行,并且根据所用的高价碘试剂,将乙酰氧基或三氟乙酰氧基引入环中。六氟异丙醇(HFIP)作为溶剂的使用至关重要。

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