首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Stereoselective syntheses of trans-fused 6,6-and 6,7-membered ether ring systems having an angular methyl group based on SmI2-induced reductive intramolecular cyclization
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Stereoselective syntheses of trans-fused 6,6-and 6,7-membered ether ring systems having an angular methyl group based on SmI2-induced reductive intramolecular cyclization

机译:基于SmI2诱导的还原性分子内环化反应的具有角甲基的6,6-和6,7-成员六元醚环系统的立体选择性合成

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摘要

Highly stereoselective syntheses of trans-fused 6,6- and 6,7-membered ether ring systems having an angular methyl group were achieved based on SmI2-induced reductive intramolecular cyclizations of an aldehyde or a methyl ketone and a beta-alkoxy acrylate. (C) 1999 Elsevier Science Ltd. All rights reserved. [References: 16]
机译:基于SmI 2诱导的醛或甲基酮和β-烷氧基丙烯酸酯的还原性分子内环化,实现了具有角甲基的反式稠合的6,6-和6,7-元醚环系统的高度立体选择性合成。 (C)1999 Elsevier ScienceLtd。保留所有权利。 [参考:16]

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