Synthetic Strategies for Cyclobutane Derivatives Without Employing [2 + 2] Cycloaddition and Their Application in Organic Synthesis

IF 2 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY ChemistrySelect Pub Date : 2025-04-24 DOI:10.1002/slct.202501056
Dr. Ram N Yadav, Dr. Md. Firoj Hossain, Prof. Dr. Subrata Ghosh
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Abstract

The cyclobutane ring stands as a remarkable structural motif, renowned for its presence in natural products and its unique reactivity in organic synthesis. Its inherent ring strain drives selective C─C bond cleavage and ring expansion, making it a compelling target for synthetic chemists. While [2 + 2] cycloaddition remains a classic method for cyclobutane construction, this approach is often unsuitable for intricately embedded cyclobutane moieties in complex natural products. To overcome these limitations, innovative synthetic strategies have been developed, bypassing direct cycloaddition to achieve precise and efficient cyclobutane assembly. This review highlights these methodologies and their transformative applications, expanding the synthetic repertoire for cyclobutane derivatives in organic chemistry.

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非[2 + 2]环加成环丁烷衍生物的合成策略及其在有机合成中的应用
环丁烷环是一个引人注目的结构基序,以其在天然产物中的存在及其在有机合成中的独特反应性而闻名。其固有的环应变驱动选择性C─C键断裂和环膨胀,使其成为合成化学家的一个引人注目的目标。虽然[2+2]环加成反应仍然是环丁烷结构的经典方法,但这种方法通常不适合复杂天然产物中错综复杂的环丁烷部分。为了克服这些局限性,已经开发了创新的合成策略,绕过直接环加成反应,实现了精确高效的环丁烷组装。本文重点介绍了这些方法及其变革性应用,扩大了有机化学中环丁烷衍生物的合成范围。
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来源期刊
ChemistrySelect
ChemistrySelect Chemistry-General Chemistry
CiteScore
3.30
自引率
4.80%
发文量
1809
审稿时长
1.6 months
期刊介绍: ChemistrySelect is the latest journal from ChemPubSoc Europe and Wiley-VCH. It offers researchers a quality society-owned journal in which to publish their work in all areas of chemistry. Manuscripts are evaluated by active researchers to ensure they add meaningfully to the scientific literature, and those accepted are processed quickly to ensure rapid online publication.
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