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首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >HETERO-1,3-DIPOLAR CYCLOADDITIONS OF DITHIOLANE-ISOCYANATE IMINIUM METHYLIDES - A NOVEL ROUTE TO 1,3-OXAZOLIDINE- AND THIAZOLIDINE-2-THIONES
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HETERO-1,3-DIPOLAR CYCLOADDITIONS OF DITHIOLANE-ISOCYANATE IMINIUM METHYLIDES - A NOVEL ROUTE TO 1,3-OXAZOLIDINE- AND THIAZOLIDINE-2-THIONES

机译:噻吩并异氰酸酯亚甲基亚胺的1,3-二氮杂酚循环-对于1,3-恶唑烷-和噻唑烷-2-硫酮的新路线

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摘要

Dithiolane- isocyanate imminium methylides which are a new type of azomethine methylide-derived 1,3-dipole undergo efficient and regioselective cycloaddition to conjugated carbonyls and thiocarbonyls to yield predominantly 1,3-oxazolidine- and thiazolidine-2-thiones formed from the initial cycloadducts via loss of thurane. [References: 13]
机译:二硫杂环戊烷-异氰酸酯亚甲基亚胺是一种新型的偶氮甲亚甲基-衍生的1,3-偶极,可进行有效的区域选择性环加成反应,生成共轭羰基和硫代羰基,主要由最初的环加合物形成1,3-恶唑烷-和噻唑烷-2-硫酮减少了硫烷。 [参考:13]

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