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NHC 催化的丙二烯酸酯的[2+2]环加成反应在取代氧杂环丁烷合成中的应用。

NHC-Catalyzed Formal [2+2] Annulations of Allenoates for the Synthesis of Substituted Oxetanes.

机构信息

Department of Chemistry, Center for Molecular Innovation and Drug Discovery , Northwestern University , Silverman Hall , Evanston , Illinois 60208 , United States.

出版信息

J Org Chem. 2018 Dec 7;83(23):14637-14645. doi: 10.1021/acs.joc.8b02464. Epub 2018 Nov 14.

Abstract

An N-heterocyclic carbene (NHC)-catalyzed reaction of γ-substituted allenoates for the synthesis of substituted oxetanes has been developed. The method provides an approach to access substituted oxetanes in a single step and is the first example of an NHC-catalyzed formal [2+2]-annulation employing γ-substituted allenoates with trifluoromethyl ketones. Mechanistic and modeling studies provide a rationale for the divergence in reactivity observed compared to the analogous reaction using unsubstituted allenoates and inform a hypothesis to explain the observed diastereoselectivity under different reaction conditions.

摘要

已开发出一种 N-杂环卡宾 (NHC) 催化的γ-取代丙二烯酸酯反应,用于合成取代的环氧乙烷。该方法提供了一种在单个步骤中获得取代的环氧乙烷的方法,并且是首例使用γ-取代的丙二烯酸酯与三氟甲基酮的 NHC 催化的形式[2+2]-环加成反应的例子。机理和模型研究为与使用未取代的丙二烯酸酯的类似反应相比观察到的反应性差异提供了依据,并提出了一个假设来解释在不同反应条件下观察到的非对映选择性。

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