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铜/钯催化的1-硅基-1,3-环己二烯的芳基硼化反应用于立体控制的多样环己烷/烯的合成。

Cu/Pd-catalyzed arylboration of a 1-silyl-1,3-cyclohexadiene for stereocontrolled and diverse cyclohexane/ene synthesis.

作者信息

Crook Phillip F, Lear Alan R, Das Suman, Brown M Kevin

机构信息

Department of Chemistry, Indiana University 800 E. Kirkwood Ave Bloomington IN 47405 USA

出版信息

Chem Sci. 2023 Sep 13;14(38):10467-10470. doi: 10.1039/d3sc02536e. eCollection 2023 Oct 4.

Abstract

The synthesis and Cu/Pd-catalyzed arylboration of 1-silyl-1,3-cyclohexadiene is described. This diene is significant as it allows for synthesis of polyfunctional cyclohexane/enes. To achieve high levels of diastereoselectivity, the use of a pyridylidene Cu-complex was employed. In addition, through the use of a chiral catalyst, an enantioselective reaction was possible. Due to the presence of the silyl and boron substituents, the products can be easily diversified into a range of valuable cyclohexane/ene products.

摘要

描述了1-硅基-1,3-环己二烯的合成及铜/钯催化的芳基硼化反应。这种二烯很重要,因为它可用于合成多官能团环己烷/烯。为实现高非对映选择性,使用了吡啶叉铜配合物。此外,通过使用手性催化剂,可实现对映选择性反应。由于存在硅基和硼取代基,产物可轻松多样化为一系列有价值的环己烷/烯产物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e2cb/10548526/feec21ec15c5/d3sc02536e-s1.jpg

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