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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 >A diastereoselective synthesis 1-trimethylsilyl-(E)-1,3-alkenynes and a simple synthesis of alkyl trimethylsilylethynyl ketones via organoboranes
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A diastereoselective synthesis 1-trimethylsilyl-(E)-1,3-alkenynes and a simple synthesis of alkyl trimethylsilylethynyl ketones via organoboranes

机译:非对映选择性合成1-三甲基甲硅烷基-(E)-1,3-烯烃和通过有机硼烷简单合成烷基三甲基甲硅烷基乙炔基酮

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摘要

A convenient,novel diastereoselective synthesis of 1-trimethylsilyl-(E)- 1,3-alkenynes and a convenient synthesis of alkyl trimethylsilylethynyl ketones based on Z-1-bromo-l-alkenylboronate esters are developed.alpha-Bromo-(Z)-l-alkenylboronate esters readily available using literature procedures smoothly undergo a reaction with trimethylsilylethynyllithium (derived from the deprotonation of trimethylsilylethyne with n-butyllithium) in tetrahydrofuran to provide the corresponding 'ate' complexes.These 'ate' complexes undergo intramolecular nucleophilic substitution reactions to afford the corresponding (E)-l-alkenylboronate esters containing trimethylsilylethynyl moiety which upon protonolysis with acetic acid provide the corresponding 1-trimethyl-silyl-(E)-l,3-alkenynes in good yields (70-82%) and in high stereochemical purities (>98%).These intermediates upon oxidation with hydrogen peroxide and sodium acetate afford the corresponding alkyl trimethylsilylethynyl ketones in good yields (66-78%).
机译:开发了一种方便,新颖的非对映选择性合成1-trimethylsilyl-((E)-1,3-alkenynes)和基于Z-1-bromo-1-alkenylboronate esters的烷基三甲基甲硅烷基乙炔基酮的便利合成方法.α-Bromo-(Z)使用文献程序容易获得的-1--1-烯基硼酸酯与三甲基硅烷基乙炔基锂(源自三甲基硅烷基乙炔与正丁基锂的去质子化)在四氢呋喃中顺利进行反应,以提供相应的``酯''配合物。这些``酯''配合物经历分子内亲核取代反应得到具有三甲基甲硅烷基乙炔基部分的相应的(E)-1-链烯基硼酸酯,其在用乙酸进行质子分解时以良好的收率(70-82%)和高产率提供了相应的1-三甲基甲硅烷基-(E)-1,3-烯炔。立体化学纯度(> 98%)。这些中间体经过氧化氢和乙酸钠氧化后,可提供相应的烷基三甲基甲硅烷基乙炔基酮,收率高s(66-78%)。

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