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首页> 外文期刊>The Journal of Organic Chemistry >Asymmetric Epoxidation of Allylic Alcohols Catalyzed by Vanadium-Binaphthylbishydroxamic Acid Complex
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Asymmetric Epoxidation of Allylic Alcohols Catalyzed by Vanadium-Binaphthylbishydroxamic Acid Complex

机译:钒-联萘基双异羟肟酸配合物催化烯丙醇的不对称环氧化

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摘要

A vanadium-binaphthylbishydroxamic acid (BBHA) complex-catalyzed asymmetric epoxidation of allylic alcohols is described. The optically active binaphthyl-based ligands BBHA 2a and 2b were synthesized from (S)-1,1'-binaphthyl-2,2'-dicarboxylic acid and N-substituted-O-trimethylsilyl (TMS)-protected hydroxylamines via a one-pot, three-step procedure. The epoxidations of 2,3,3-trisubstituted allylic alcohols using the vanadium complex of 2a were easily performed in toluene with a TBHP water solution to afford (2R)-epoxy alcohols in good to excellent enantioselectivities.
机译:描述了钒-联萘基双异羟肟酸(BBHA)络合物催化的烯丙醇的不对称环氧化。由(S)-1,1'-联萘-2,2'-二羧酸和N-取代-O-三甲基甲硅烷基(TMS)保护的羟胺通过单-羟基合成旋光的基于联萘的配体BBHA 2a和2b。锅,分三步操作。使用2a的钒配合物,在TBHP水溶液中轻松地进行使用2a的钒配合物进行的2,3,3-三取代的烯丙醇的环氧化,可制得具有良好对映选择性的(2R)-环氧醇。

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