首页> 外文期刊>Chemical Communications >Chiral tertiary 2-furyl alcohols: diversified key intermediates to bioactive compounds. Their enantioselective synthesis via (2-furyl)aluminium addition to ketones catalyzed by a titanium catalyst of (S)-BINOL
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Chiral tertiary 2-furyl alcohols: diversified key intermediates to bioactive compounds. Their enantioselective synthesis via (2-furyl)aluminium addition to ketones catalyzed by a titanium catalyst of (S)-BINOL

机译:手性2-呋喃叔醇:生物活性化合物的多种关键中间体。通过(S)-BINOL的钛催化剂催化的酮类中的(2-呋喃基)铝加成反应生成对映体

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摘要

Novel asymmetric 2-furyl additions of (2-furyl)AlEt_2(THF) to aromatic ketones and one α,β-unsaturated ketone catalyzed by a titanium catalyst of 10-20 mol% (5)-BINOL are reported to furnish tertiary furyl alcohols in good to excellent enantioselec-tiviti
机译:据报道,在芳族酮中有新型的(2-呋喃基)AlEt_2(THF)不对称的2-呋喃基化合物和一种由10-20 mol%(5)-BINOL的钛催化剂催化的α,β-不饱和酮。从优秀到优秀的对映体

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