首页> 外文OA文献 >Stereospecific 3+2 cycloaddition of 1,2-cyclopropanated sugars and ketones catalyzed by SnCl4: an efficient synthesis of multi-substituted perhydrofuro2,3-bfurans and perhydrofuro2,3-bpyrans
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Stereospecific 3+2 cycloaddition of 1,2-cyclopropanated sugars and ketones catalyzed by SnCl4: an efficient synthesis of multi-substituted perhydrofuro2,3-bfurans and perhydrofuro2,3-bpyrans

机译:SnCl4催化1,2,2-环丙烷化糖和酮的立体特异性3 + 2环加成反应:多取代全氢呋喃2,3-b呋喃和全氢呋喃2,3-b吡喃的有效合成

摘要

Stereospecific [3+2] cycloaddition of 1,2-cyclopropanated sugars and ketones catalyzed by SnCl4 is described. The method offers multi-substituted perhydrofuro[2,3-b]furans (bis-THFs) and perhydrofuro[2,3-b]pyrans containing a quaternary carbon chiral center in good to excellent yields.
机译:描述了SnCl4催化的1,2-环丙烷化糖和酮的立体特异性[3 + 2]环加成。该方法提供了具有季碳手性中心的多取代的全氢呋喃[2,3-b]呋喃(双-THF)和全氢呋喃[2,3-b]吡喃,产率高至优异。

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