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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 >Highly stereoselective method to prepare bis-phenylchalcogen alkenes via addition of chalcogenolate to phenylseleno alkynes
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Highly stereoselective method to prepare bis-phenylchalcogen alkenes via addition of chalcogenolate to phenylseleno alkynes

机译:通过将硫族油酸酯加入苯基硒代炔烃中来制备双苯基硫属元素烃的高度立体选择性方法

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摘要

The preparation of bis-phenylchalcogen alkenes starting from phenylseleno alkynes is described. The nucleophilic species of selenium, tellurium and sulfur were generated in situ from the reaction of the respective diphenyl dichalcogenide with NaBH4 in PEG-400 as solvent. The chalcogenolate anions were efficiently and selectively added to a variety of phenylselenoalkynes at mild conditions, furnishing the respective (Z)-1,2-bis-phenylchalcogen alkenes in good yields.
机译:描述了从苯基硒代炔烃开始制备双苯基硫属元素烯烃。硒,碲和硫的亲核物种是由各自的二苯基二硫代硫酸钠与NaBH4在PEG-400中作为溶剂的反应原位生成的。在温和的条件下,将硫属元素化物阴离子有效且选择性地添加到各种苯基硒代炔烃中,从而以良好的收率提供了各自的(Z)-1,2-双-苯基硫属元素烃。

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