首页> 外文期刊>Tetrahedron >Facile synthesis of sulfenyl-substituted isocoumarins, heterocycle-fused pyrones and 3-(inden-1-ylidene)isobenzofuranones by FeCl _3-promoted regioselective annulation of o-(1-alkynyl)benzoates and o-(1-alkynyl) heterocyclic carboxylates with disulfides
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Facile synthesis of sulfenyl-substituted isocoumarins, heterocycle-fused pyrones and 3-(inden-1-ylidene)isobenzofuranones by FeCl _3-promoted regioselective annulation of o-(1-alkynyl)benzoates and o-(1-alkynyl) heterocyclic carboxylates with disulfides

机译:FeCl _3-促进邻-(1-炔基)苯甲酸酯和邻-(1-炔基)杂环羧酸酯的区域选择性环化反应,可轻松合成亚磺酰基取代的异香豆素,杂环稠合的吡喃酮和3-(茚-1-基)异苯并呋喃酮二硫化物

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摘要

Reported herein is the FeCl _3-promoted intermolecular sulfoesterification of o-(1-alkynyl)benzoates with disulfides, which provides a convenient and efficient method for synthesis of 4-sulfenylisocoumarins. Various functional groups such as methoxy, halides, ester, cyano and silicon groups in the substrates are tolerated, and heterocycle-fused chalcogenylpyrones are also successfully achieved directly from the corresponding heterocyclic precursors under the same reaction conditions. In addition, starting from diynylbenzoate, this reaction sequence can be combined with a bicyclization step leading to the tetracyclic (E)-3-(2-phenyl-3-phenylchalcogenylinden-1-ylidene)isobenzofuranone frameworks with high regiospecificity and exclusive trans stereoselectivity.
机译:本文报道了邻二(1-炔基)苯甲酸酯与二硫化物的FeCl 3促进的分子间磺基酯化,其提供了合成4-亚硫基异香豆素的方便有效的方法。可以耐受底物中的各种官能团,例如甲氧基,卤化物,酯,氰基和硅基团,并且在相同的反应条件下,还可以直接从相应的杂环前体成功地实现杂环稠合的硫属酰基吡喃酮。另外,从二炔基苯甲酸酯开始,该反应序列可以与双环化步骤结合,从而导致具有高区域特异性和排他立体选择性的四环(E)-3-(2-苯基-3-苯基硫族y基-芳基-1-亚烷基)异苯并呋喃酮骨架。

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