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α,β-不饱和羰基锆化合物的合成及其在高选择合成中的应用

A Stereoselective Synthetic Route to (E)- α,β-Unsaturated Thioesters
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摘要 由端炔和Cp2Zr(H)Cl(Cp=η5-C5H5)及CO反应,得到α,β-不饱和羰基锆化合物,进而与芳基硫 氯反应,合成了α,β-不饱和羧酸硫酯,产率中等至良好. Terminal alkynes 1 react with Cp2Zr(H)Cl (Cp = η 5-C5H5) and CO to give acylzirconocene chloride derivatives 2, which are trapped with arylsulfenyl chloride to afford (E)- α,β-unsaturated thioesters 3.
作者 钟平
出处 《温州师范学院学报》 2002年第6期31-34,共4页 Journal of Wenzhou Teachers College(Philosophy and Social Science Edition)
基金 国家自然科学基金(20272045) 浙江省自然科学基金资助课题(201015)
关键词 α β-不饱和羰基锆化合物 高选择合成 端炔 芳基硫氯 α β-不饱和羧酸硫酯 锆氢化反应 合成反应 terminal alkynes arylsulfenyl chloride α,β-unsaturated thioesters hydrozirconation
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参考文献12

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