手性双恶唑-铜(II)配合物催化中羟基苯甲酸反对称单磺化一锅法合成反式二苯乙烯氧化物

IF 1.5 4区 化学 Q3 CHEMISTRY, ORGANIC
Kenji Yatsuzuka, Midori Kawasaki, Ryuichi Shirai
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引用次数: 0

摘要

手性苯乙烯氧化物是合成不对称催化的手性配体、非对映选择性转化的手性助剂和许多化合物的手性构建块的前体的有用的多功能中间体。我们通过手性配体- cucl2配合物催化中邻苯二甲酸酯的对映选择性不对称甲基化反应,然后在碱基促进的分子内环化反应,在一锅操作中获得了高收率的反式二苯乙烯氧化物,对映选择性高达99% ee。这种简单的转化为不对称合成高光学纯度的二苯乙烯氧化物提供了最可行和最有前途的选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Asymmetric one-pot synthesis of trans-stilbene oxide via desymmetrizing monosulfonylation of meso-hydrobenzoin catalyzed by a chiral bisoxazoline–copper (II) complex

Asymmetric one-pot synthesis of trans-stilbene oxide via desymmetrizing monosulfonylation of meso-hydrobenzoin catalyzed by a chiral bisoxazoline–copper (II) complex
Chiral stilbene oxides are useful and versatile intermediates for the synthesis of chiral ligands for asymmetric catalysis, chiral auxiliaries for diastereoselective transformations, and precursors for chiral building blocks of many compounds. We achieved the enantioselective desymmetric tosylation of meso-hydrobenzoin catalyzed by a chiral ligand–CuCl2 complex followed by base promoted intramolecular cyclization to furnish trans-stilbene oxide in high yield with excellent enantioselectivity up to 99 %ee in a one-pot operation. This simple transformation offers the most feasible and promising option for the asymmetric synthesis of stilbene oxides with high optical purity.
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来源期刊
Tetrahedron Letters
Tetrahedron Letters 化学-有机化学
CiteScore
3.50
自引率
5.60%
发文量
521
审稿时长
28 days
期刊介绍: Tetrahedron Letters provides maximum dissemination of outstanding developments in organic chemistry. The journal is published weekly and covers developments in techniques, structures, methods and conclusions in experimental and theoretical organic chemistry. Rapid publication of timely and significant research results enables researchers from all over the world to transmit quickly their new contributions to large, international audiences.
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