吡啶1,n-两性离子(n=4和5)环化反应的最新进展:范围和机理

Jiali Huang , Lei Zhang , Xiangtai Meng
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引用次数: 1

摘要

含氮含硫杂环化合物广泛存在于具有生物活性的天然产物和药物分子中,具有独特的生物活性。在过去的几十年里,人们一直致力于开发方便有效的合成这些化合物的策略。吡啶两性离子具有独特的反应活性,在构建含氮和含硫杂环中发挥着重要作用。近年来,吡啶两性离子在环化反应中被广泛用于合成新型杂环化合物。本文综述了吡啶1,n-两性离子(n=4和5)环化反应的最新进展,并重点介绍了这些两性离子在高效构建杂环中的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Recent advances in the cyclization reactions of pyridinium 1,n-zwitterions (n = 4 and 5): scope and mechanism

Recent advances in the cyclization reactions of pyridinium 1,n-zwitterions (n = 4 and 5): scope and mechanism

Nitrogen- and sulfur-containing heterocyclic compounds widely exist in bioactive natural products and drug molecules with unique bioactivity. In the past few decades, great efforts have been devoted to developing convenient and efficient strategies for the synthesis of these compounds. Pyridinium zwitterions with unique reactivity play a significant role in the construction of nitrogen- and sulfur-containing heterocycles. In recent years, pyridinium zwitterions have been extensively used in cyclization reactions for the synthesis of novel heterocyclic compounds. This review summarizes the recent advances in cyclization reactions involving pyridinium 1,n-zwitterions (n = 4 and 5) and highlights the applications of these zwitterions in the efficient construction of heterocycles.

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