Zhang Fuhao, Dutta Subhabrata, Petti Alessia, Rana Debanjan, Daniliuc Constantin G, Glorius Frank
Organisch-Chemisches Institut, Universität Münster, Corrensstraße 36, 48149, Münster, Germany.
Angew Chem Int Ed Engl. 2025 Feb 3;64(6):e202418239. doi: 10.1002/anie.202418239. Epub 2025 Jan 5.
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.
双环[1.1.0]丁烷(BCBs)最近作为一种通用前体引起了广泛的研究兴趣,可用于以直接且原子经济的方式合成潜在的[n.1.1]生物电子等排体和多官能化环丁烷。在此,我们报道了一种溶剂依赖性的BCBs发散环化反应,该反应可提供高度非对映选择性的修饰环丁烷和含氧双环[3.1.1]庚烷(BCHeps),它们可作为间位取代芳烃的生物电子等排体。此外,还探索了一种前所未有的BCBs 1,2-双官能化反应模式,从而扩展了芳烃生物电子等排体和高度官能化环丁烷的化学空间。