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联合动态动力学拆分与 C-H 官能化反应实现非联芳轴手性有机硅烷的简便合成。

Combined Dynamic Kinetic Resolution and C-H Functionalization for Facile Synthesis of Non-Biaryl-Atropisomer-Type Axially Chiral Organosilanes.

机构信息

Key Laboratory of Organosilicon Chemistry and Material Technology of Ministry of Education, and Key Laboratory of Organosilicon Material Technology of Zhejiang Province, Hangzhou Normal University, No. 2318, Yuhangtang Road, Hangzhou, 311121, P. R. China.

State Key Laboratory for Oxo Synthesis and Selective Oxidation, Suzhou Research Institute and Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Hangzhou, 311121, P. R. China.

出版信息

Chemistry. 2021 Mar 1;27(13):4336-4340. doi: 10.1002/chem.202100237. Epub 2021 Feb 8.

Abstract

Although asymmetric C-H functionalization has been available for the synthesis of structurally diverse molecules, catalytic dynamic kinetic resolution (DKR) approaches to change racemic stereogenic axes remain synthetic challenges in this field. Here, a concise palladium-catalyzed DKR was combined with C-H functionalization involving olefination and alkynylation for the highly efficient synthesis of non-biaryl-atropisomer-type (NBA) axially chiral oragnosilanes. The chemistry proceeded through two different and distinct DKR: first, an atroposelective C-H olefination or alkynylation produced axially chiral vinylsilanes or alkynylsilanes as a new family of non-biaryl atropisomers (NBA), and second, the extension of this DKR strategy to twofold o,o'-C-H functionalization led to the multifunctional axially chiral organosilicon compounds with up to >99 % ee.

摘要

虽然不对称 C-H 功能化可用于合成结构多样的分子,但在该领域中,催化动态动力学拆分 (DKR) 方法来改变外消旋立体轴仍然是合成挑战。在这里,我们将简洁的钯催化 DKR 与涉及烯烃和亲核加成的 C-H 功能化相结合,以高效合成非联芳型轴手性有机硅烷。该反应通过两种不同且独特的 DKR 进行:首先,对映选择性 C-H 烯烃化或炔烃化生成轴手性乙烯基硅烷或炔基硅烷,作为新的非联芳轴手性异构体 (NBA) 家族;其次,将这种 DKR 策略扩展到两倍的 o,o'-C-H 功能化,导致具有高达 >99%ee 的多功能轴手性有机硅化合物。

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