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通过NHC生成的炔基酰唑鎓与苯并恶唑基乙酸酯的形式[3 + 3]环化反应催化合成1-苯并恶唑并[3,2-]吡啶-1-酮及其光物理研究

Catalytic Synthesis of 1-Benzoxazolo[3,2-]pyridin-1-ones via Formal [3 + 3] Annulations of NHC-Generated Alkynyl Acylazoliums with Benzoxazolyl Acetates and Their Photophysical Studies.

作者信息

Sarkar Sibasis, Das Suravi, Gandhi Shikha

机构信息

Department of Chemical Sciences, Indian Institute of Science Education and Research Berhampur, Berhampur, Odisha 760010, India.

出版信息

J Org Chem. 2024 Nov 1;89(21):15559-15567. doi: 10.1021/acs.joc.4c01616. Epub 2024 Oct 21.

Abstract

We disclose the synthesis of a tricyclic fused N-heterocycle via the NHC-catalyzed annulation of either a ynal or an alkynyl ester with readily accessible benzoxazolyl acetate. While the annulation with ynals requires an oxidant, the reaction with alkynyl esters proceeds via the direct generation of alkynyl acylazolium intermediates with an NHC. With the dearth of catalytic processes to access these 1-benzoxazolo[3,2-]pyridin-1-ones from simple starting materials, this method is especially important. The photophysical properties of the products have also been evaluated.

摘要

我们报道了通过氮杂环卡宾(NHC)催化的烯炔或炔基酯与易于获得的乙酸苯并恶唑酯的环化反应合成三环稠合氮杂环。虽然烯炔的环化反应需要氧化剂,但炔基酯的反应是通过与NHC直接生成炔基酰基唑鎓中间体进行的。由于缺乏从简单原料制备这些1-苯并恶唑并[3,2 -]吡啶-1-酮的催化方法,该方法尤为重要。还对产物的光物理性质进行了评估。

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