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Efficient Synthesis of Chiral Trisubstituted 12‐Allenyl Ketones by Catalytic Asymmetric Conjugate Addition of Malonic Esters to Enynes

机译:丙二酸酯向烯炔的催化不对称共轭加成反应高效合成手性三取代12-烯基酮

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摘要

An N,N′‐dioxide/scandium(III) complex catalyzed, highly efficient conjugate addition of malonic esters to enynes is described. A range of trisubstituted 1,2‐allenyl ketones were obtained in high yields (up to 99 %) with good d.r. (up to 95/5) and excellent ee values (97 %–99 %). Moreover, the products could be easily transformed into chiral furan and 5‐hydroxypyrazoline derivatives, both of which are important skeletons of many biologically active compounds and pharmacologicals.
机译:描述了N,N'-二氧化物/ scan(III)络合物催化丙二酸酯向烯炔的高效共轭加成。以高收率(d.r.)获得了一系列三取代的1,2-烯丙基酮(产率高达99%)。 (最高95/5)和出色的ee值(97%–99%)。而且,这些产物很容易转化为手性呋喃和5-羟基吡唑啉衍生物,它们都是许多生物活性化合物和药理学的重要骨架。

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