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立体选择性烯烃复分解反应:通向动力学选择性的途径。

Stereoretentive Olefin Metathesis: An Avenue to Kinetic Selectivity.

机构信息

Division of Chemistry and Chemical Engineering, California Institute of Technology, 1200 E California Blvd., Pasadena, CA, 91125, USA.

出版信息

Angew Chem Int Ed Engl. 2017 Sep 4;56(37):11024-11036. doi: 10.1002/anie.201704686. Epub 2017 Jul 26.

Abstract

Olefin metathesis is an incredibly valuable transformation that has gained widespread use in both academic and industrial settings. Lately, stereoretentive olefin metathesis has garnered much attention as a method for the selective generation of both E- and Z-olefins. Early studies employing ill-defined catalysts showed evidence for retention of the stereochemistry of the starting olefins at low conversion. However, thermodynamic ratios E/Z were reached as the reaction proceeded to equilibrium. Recent studies in olefin metathesis have focused on the synthesis of catalysts that can overcome the inherent thermodynamic preference of an olefin, providing synthetically useful quantities of a kinetically favored olefin isomer. These reports have led to the development of stereoretentive catalysts that not only generate Z-olefins selectively, but also kinetically produce E-olefins, a previously unmet challenge in olefin metathesis. Advancements in stereoretentive olefin metathesis using tungsten, ruthenium, and molybdenum catalysts are presented.

摘要

烯烃复分解是一种非常有价值的转化反应,在学术和工业领域都得到了广泛的应用。最近,立体选择性烯烃复分解作为一种选择性生成 E-和 Z-烯烃的方法引起了广泛关注。早期使用未明确定义的催化剂的研究表明,在低转化率下,起始烯烃的立体化学可以得到保留。然而,随着反应达到平衡,热力学比例 E/Z 达到。最近烯烃复分解的研究集中在合成可以克服烯烃固有热力学偏好的催化剂上,从而提供具有合成用途的动力学有利烯烃异构体的大量产物。这些报告导致了立体选择性催化剂的发展,这些催化剂不仅可以选择性地生成 Z-烯烃,而且还可以动力学地生成 E-烯烃,这是烯烃复分解中以前未满足的挑战。本文介绍了使用钨、钌和钼催化剂的立体选择性烯烃复分解的进展。

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