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杂环合成的最新进展:吡啶翁和喹啉翁 1,4-内盐的环化反应。

Recent Progress in Heterocycle Synthesis: Cyclization Reaction with Pyridinium and Quinolinium 1,4-Zwitterions.

机构信息

Innovation Research Center of Chiral Drugs, Institute for Advanced Study, Chengdu University, Chengdu 610106, China.

出版信息

Molecules. 2023 Mar 29;28(7):3059. doi: 10.3390/molecules28073059.

Abstract

Heteroarene 1, n-zwitterions are powerful and versatile building blocks in the construction of heterocycles and have received increasing attention in recent years. In particular, pyridinium and quinolinium 1,4-zwitterions have been widely studied and used in a variety of cyclization reactions due to their air stability, ease of use, and high efficiency. Sulfur- and nitrogen-based pyridinium and quinolinium 1,4-zwitterions, types of emerging heteroatom-containing synthons, have attracted much attention from chemists. These 1,4-zwitterions, which contain multiple reaction sites, have been successfully used in the synthesis of three- to eight-membered cyclic compounds over the last decade. In this review, we present the exciting progress made in the field of cyclization reactions of sulfur- and nitrogen-based pyridinium and quinolinium 1,4-zwitterions. Moreover, the mechanistic insights, the transition states, some synthetic applications, and the challenges and opportunities are also discussed. We hope to provide an overview for synthetic chemists who are interested in the heterocycle synthesis from cyclization reaction with pyridinium and quinolinium 1,4-zwitterions pyridinium and quinolinium 1,4-zwitterions.

摘要

杂芳族 1,n-两性离子是构建杂环的强大且多功能的构建块,近年来受到越来越多的关注。特别是,由于吡啶鎓和喹啉鎓 1,4-两性离子的空气稳定性、易用性和高效率,它们已被广泛研究并用于各种环化反应中。基于硫和氮的吡啶鎓和喹啉鎓 1,4-两性离子,作为新兴的含杂原子的缩合试剂类型,引起了化学家的广泛关注。这些含有多个反应位点的 1,4-两性离子,在过去十年中已成功用于合成三至八元环状化合物。在本文综述中,我们介绍了基于硫和氮的吡啶鎓和喹啉鎓 1,4-两性离子的环化反应领域令人兴奋的进展。此外,还讨论了反应机理、过渡态、一些合成应用以及挑战和机遇。我们希望为有兴趣从吡啶鎓和喹啉鎓 1,4-两性离子的环化反应中合成杂环的合成化学家提供一个概述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fac0/10095670/f21078f3719d/molecules-28-03059-g001.jpg

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