Solvent-Dependent Divergent Cyclization of Bicyclo[1.1.0]butanes

IF 16.9 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Angewandte Chemie International Edition Pub Date : 2024-12-17 DOI:10.1002/anie.202418239
Dr. Fuhao Zhang, Dr. Subhabrata Dutta, Dr. Alessia Petti, Debanjan Rana, Dr. Constantin G. Daniliuc, Prof. Dr. Frank Glorius
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Abstract

Bicyclo[1.1.0]butanes (BCBs) have recently garnered significant research interest as versatile precursors for synthesizing potential [n.1.1] bioisosteres and multi-functionalized cyclobutanes in a straightforward and atom-economical manner. Here, we report a solvent-dependent divergent cyclization of BCBs that provides highly diastereospecific decorated cyclobutanes and oxygen-containing bicyclo[3.1.1]heptanes (BCHeps), which serve as bioisosteres of meta-substituted arenes. Additionally, an unprecedented 1,2-difunctionalization reaction mode for BCBs was explored, thus expanding the chemical space of arene bioisosteres and highly functionalized cyclobutanes.

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双环[1.1.0]丁烷的溶剂依赖性发散环化
双环[1.1.0]丁烷(BCBs)作为一种多功能前体,以直接和原子经济的方式合成潜在的[n.1.1]生物异构体和多功能环丁烷,最近引起了研究人员的极大兴趣。在此,我们报告了一种依赖溶剂的 BCB 发散环化方法,该方法可提供高度非对映特异性的装饰环丁烷和含氧双环[3.1.1]庚烷(BCHeps),这些环丁烷和含氧双环[3.1.1]庚烷可作为元取代烷的生物异构体。这种新颖的策略采用了精确的定向控制,以实现理想的发散。此外,还探索了一种前所未有的 BCB 1,2-二官能化反应模式,拓展了有效探索炔类生物异构体和高官能环丁烷化学空间的可用方法。
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来源期刊
CiteScore
26.60
自引率
6.60%
发文量
3549
审稿时长
1.5 months
期刊介绍: Angewandte Chemie, a journal of the German Chemical Society (GDCh), maintains a leading position among scholarly journals in general chemistry with an impressive Impact Factor of 16.6 (2022 Journal Citation Reports, Clarivate, 2023). Published weekly in a reader-friendly format, it features new articles almost every day. Established in 1887, Angewandte Chemie is a prominent chemistry journal, offering a dynamic blend of Review-type articles, Highlights, Communications, and Research Articles on a weekly basis, making it unique in the field.
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