首页> 外文期刊>The Journal of Organic Chemistry >5-and 6-exocyclic products, cis-2,3,5-trisubstituted tetrahydrofurans, and cis-2,3,6-trisubstituted tetrahydropyrans via Prins-type cyclization
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5-and 6-exocyclic products, cis-2,3,5-trisubstituted tetrahydrofurans, and cis-2,3,6-trisubstituted tetrahydropyrans via Prins-type cyclization

机译:通过Prins型环化作用的5和6外环产物,顺式2,3,5-三取代的四氢呋喃和顺式2,3,6-三取代的四氢吡喃

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摘要

Exocyclic proc [GRAPHICS] alkynyl alcohols with various aldehydes via Prins-type cyclization in good yields. It is of interest that synthesized 5- and 6-exocyclic vinyl cations generated as a result of Prins-type cyclization could be trapped as a vinyl triflate in CH2Cl2 to give 3-furanylidenes and 3-pyranylidenes. Those 3-furanylidenes and 3-pyranylidenes underwent hydrolysis to give the corresponding 3-acyl-substituted products having all-cis-configured isomers, such as 2,3,5-trisubstituted tetrahydrofurans and 2,3,6-trisubstituted tetrahydropyrans.
机译:通过Prins型环化反应得到的带有各种醛的环外proc [GRAPHICS]炔醇,收率很高。令人感兴趣的是,由于Prins型环化而生成的合成的5-和6-环外乙烯基阳离子可能会被捕获为三氟甲磺酸乙烯酯,并存在CH2Cl2中,从而生成3-呋喃基和3-吡喃基。将那些3-呋喃基亚烷基和3-吡喃基亚胺水解,得到具有全顺式构型的异构体的相应的3-酰基取代的产物,例如2,3,5-三取代的四氢呋喃和2,3,6-三取代的四氢吡喃。

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