首页> 外文期刊>Synthetic Communications >P2O5-promoted efficient and diastereoselective synthesis of substituted 5-methylene-dihydropyran-2,6-diones and 3-methylene-3,4-dihydropyran-2-ones
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P2O5-promoted efficient and diastereoselective synthesis of substituted 5-methylene-dihydropyran-2,6-diones and 3-methylene-3,4-dihydropyran-2-ones

机译:P2O5促进高效和非对映选择性合成取代的5-亚甲基-二氢吡喃-2,6-二酮和3-亚甲基-3,4-二氢吡喃-2-酮

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摘要

A simple, efficient, and diastereoselective synthesis of 5-methylene-dihydropyran-2,6-diones and 3-methylene-3,4-dihydropyran-2-ones from substrates afforded by the S-N(2) reaction between the acetyl derivatives of the Baylis-Hillman adducts and methylacetoacetate or acetylacetone or benzoyl acetone via saponification followed by P2O5-mediated cyclization is described.
机译:简单,有效和非对映选择性合成5-亚甲基-二氢吡喃-2,6-二酮和3-亚甲基-3,4-二氢吡喃-2-酮从底物的乙酰基衍生物之间的SN(2)反应提供描述了通过皂化,然后是P 2 O 5介导的环化作用的Baylis-Hillman加合物和乙酰乙酸甲酯或乙酰丙酮或苯甲酰基丙酮。

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