Liu Gang, Shi Zhaoxin, Guo Chuning, Gu Danyu, Wang Zhaobin
Key Laboratory of Precise Synthesis of Functional Molecules of Zhejiang Province, Department of Chemistry, School of Science, Westlake University, Hangzhou, 310030, Zhejiang Province, China.
Key Laboratory of Precise Synthesis of Functional Molecules of Zhejiang Province, Instrumentation and Service Center for Molecular Sciences, Westlake University, Hangzhou, 310024, Zhejiang Province, China.
Angew Chem Int Ed Engl. 2025 Feb 3;64(6):e202418746. doi: 10.1002/anie.202418746. Epub 2025 Jan 16.
Efficient methods for synthesizing allenes from readily available starting materials pose a persistent challenge in organic chemistry. In this work, we present a novel two-stage protocol for allene synthesis involving the single-atom insertion into alkenes, facilitated by synergistic photoredox and cobalt catalysis. Diverging from conventional methods such as the Doering-LaFlamme reaction, this photochemical rearrangement approach operates efficiently under mild conditions in a radical-based manner. The protocol exhibits a broad substrate scope and demonstrates applicability in the late-stage diversification of alkene-containing natural products and bioactive molecules. Preliminary mechanistic studies and density functional theory (DFT) calculations offer insights into the reaction pathway, indicating a radical mechanism involving fleeting cyclopropyl carbene intermediates followed by rapid ring opening to form allenes.
从易得的起始原料合成丙二烯的有效方法一直是有机化学中的一项持续性挑战。在这项工作中,我们提出了一种新颖的丙二烯合成两步法,该方法涉及通过协同光氧化还原和钴催化将单原子插入烯烃中。与诸如杜林-拉弗拉姆反应等传统方法不同,这种光化学重排方法在温和条件下以自由基方式高效运行。该方法具有广泛的底物范围,并证明了其在含烯烃天然产物和生物活性分子后期多样化中的适用性。初步的机理研究和密度泛函理论(DFT)计算为反应途径提供了见解,表明这是一种涉及短暂环丙基卡宾中间体然后快速开环形成丙二烯的自由基机理。