环链同分异构。I:带一个杂原子的杂环的合成应用(综述)

IF 0.8 4区 化学 Q4 CHEMISTRY, ORGANIC Russian Journal of Organic Chemistry Pub Date : 2024-10-14 DOI:10.1134/S107042802407025X
M. Abdel-Megid, T. E. Ali, A. E. Rashad, A. H. Shamroukh
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引用次数: 0

摘要

由于开环或环化而导致异构化的分子间排列称为环链同分异构。本文讨论了通过环链同分异构现象形成的一些具有一个杂原子的重要杂环化合物。大多数含氧或含氮杂环系统都以分离、缩合或斯派罗形式出现。本综述根据杂原子与杂多原子键分子内加成形成的杂环的大小,用 3 到 6 的数字前缀表示。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Ring-Chain Tautomerism. I: Synthetic Applications of Heterocycles with One Heteroatom (A Review)

The intermolecular arrangements leading to isomerization due to ring opening or cyclization is known as ring−chain tautomerism. The formation of some important heterocyclic compounds having one heteroatom via ring-chain tautomeric phenomenon is discussed. Most oxygenated or nitrogenous heterocyclic systems appeared isolated, condensed or in Spiro form. According to the size of the heterocyclic ring being formed via intramolecular addition of a heteroatom to a heteropolar multiple bond, indicated by a numerical prefix from three to six is reported in this review.

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来源期刊
CiteScore
1.40
自引率
25.00%
发文量
139
审稿时长
3-6 weeks
期刊介绍: Russian Journal of Organic Chemistry is an international peer reviewed journal that covers all aspects of modern organic chemistry including organic synthesis, theoretical organic chemistry, structure and mechanism, and the application of organometallic compounds in organic synthesis.
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