有机化学 ›› 2026, Vol. 46 ›› Issue (5): 2031-2035.DOI: 10.6023/cjoc202510034 上一篇    下一篇

研究论文

Turbo格氏试剂介导的酰基硅羰基还原反应

郭子心, 许盼, 徐晓锋, 刘振兴*()   

  1. 郑州大学化学学院 郑州 450001
  • 收稿日期:2025-10-31 修回日期:2026-02-01 发布日期:2026-03-06
  • 作者简介:

    †共同第一作者

  • 基金资助:
    河南省自然科学基金(232300421087); 郑州大学青年骨干教师培养计划(2025ZDGGJS025)

Carbonyl Reduction of Acylsilanes Mediated by Turbo Grignard

Zixin Guo, Pan Xu, Xiaofeng Xu, Zhenxing Liu*()   

  1. College of Chemistry, Zhengzhou University, Zhengzhou 450001
  • Received:2025-10-31 Revised:2026-02-01 Published:2026-03-06
  • Contact: * E-mail: liuzhenxing@zzu.edu.cn
  • About author:

    These authors contributed equally to this work

  • Supported by:
    Natural Science Foundation of Henan Province(232300421087); Training Program for Young Backbone Teachers in Higher Education Institutions of Zhengzhou University(2025ZDGGJS025)

发展了室温下Turbo格氏试剂介导的酰基硅烷的羰基碳还原反应. 该反应适用于芳基、炔基和烷基取代的酰基硅, 分离收率最高可达99%, 并且官能团耐受性好, 双键、叁键和卤素等均能兼容. 反应也适用于多酰基硅的还原, 进一步增强了其合成实用性.

关键词: Turbo格氏试剂, 酰基硅, 还原反应, α-硅基醇

This paper presents the development of a carbonyl carbon reduction reaction of acylsilanes mediated by Turbo Grignard reagents at room temperature. The reaction is applicable to aryl-, alkynyl-, and alkyl-substituted acylsilanes, achieving isolated yields of up to 99% with good functional group tolerance. Various functional groups, including carbon-carbon double bonds, triple bonds, and halogens, are compatible under the reaction conditions. The method is also suitable for the reduction of polyacylsilanes, further enhancing its synthetic utility.

Key words: Turbo Grignard, acylsilane, reduction, α-silyl alcohol