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Studies in Asymmetric Epoxidation of Chalcone Using Quaternary Salts and Nonionic Surfactants Based on 6-Amino-6-deoxy-glucose as Chiral Phase Transfer Catalysts

机译:基于6-氨基-6-脱氧 - 葡萄糖的季盐和非离子表面活性剂作为手性相转移催化剂的不对称环氧化研究

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Quaternary salts and nonionic surfactants based on 6-amino-6-deoxy-glucose were explored as chiral phase transfer catalysts for the asymmetric epoxidation of chalcone. Quaternary salts used in the present study, were void of any branched chain or long hydrocarbon chain, whereas the sugar based nonionic surfactants have a long hexadecyl moiety as tail. It was observed that quaternary salts showed no activity as phase transfer catalysts but sugar based nonionic surfactants acted as chiral phase transfer catalysts. It was also revealed that hydrophilicity of the surfactant favors more yield whereas stereochemistry governs enantioselectivity. (6,6'-Hexadecylimino) bis(6-deoxy-1,2-O-isopropylidene-α-D-glucofuranose) was found to be the most suitable chiral phase transfer catalyst, resulting asymmetric epoxidation of chalcone with 90% yield and 16.5% enantiomeric excess (ee).
机译:基于6-氨基-6-脱氧 - 葡萄糖的季盐和非离子表面活性剂被探索为Chalcone的不对称环氧化的手性相转移催化剂。本研究中使用的季盐是任何支链或长烃链的空隙,而糖的非离子表面活性剂具有长的十六烷基部分作为尾部。观察到季盐显示不作为相转移催化剂的活性,但是糖基的非离子表面活性剂作用为手性相转移催化剂。还揭示了表面活性剂的亲水性更加屈服,而立体化治理对映选择性。 (6,6,6'-十六烷基氨基氨基)发现双(6-脱氧-1,2- o-异丙基甲苯-1-D-葡糖酚呋喃)是最合适的手性相转移催化剂,导致Chalcone的不对称环氧化,产率90% 16.5%对映体过量(EE)。

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