Chinese Journal of Organic Chemistry ›› 2026, Vol. 46 ›› Issue (3): 1027-1038.DOI: 10.6023/cjoc202508021 Previous Articles     Next Articles

ARTICLES

镁促进未保护的吲哚及喹喔啉衍生物的选择性还原

韦娜娜, 郭婉真, 鲁星, 任志强, 马豪杰, 张玉琦, 王记江, 韩波*()   

  1. 延安大学化学与化工学院新能源新功能材料重点实验室 陕西省化学反应工程重点实验室 陕西延安 716000
  • 收稿日期:2025-08-25 修回日期:2025-10-26 发布日期:2025-11-27
  • 通讯作者: 韩波
  • 基金资助:
    国家自然科学基金(22061041)

Magnesium-Promoted Selectively Reduction of Unprotected Indoles and Quinoxalines

Nana Wei, Wanzhen Guo, Xing Lu, Zhiqiang Ren, Haojie Ma, Yuqi Zhang, Jijiang Wang, Bo Han*()   

  1. Shaanxi Key Laboratory of Chemical and Reaction Engineering, Laboratory of New Energy & New Function Materials, College of Chemistry and Chemical Engineering, Yan'an University, Yan'an, Shaanxi 716000
  • Received:2025-08-25 Revised:2025-10-26 Published:2025-11-27
  • Contact: Bo Han
  • Supported by:
    National Natural Science Foundation of China(22061041)

This study present a transfer hydrogenation method employing ammonia borane (H3N•BH3) as the hydrogen source and inexpensive magnesium as the catalyst for the selective reduction of unprotected indoles, quinoxalines, benzoxazole, benzothiazole, quinolines, and their derivatives, resulting the corresponding alicyclic heterocyclic compounds with desirable yields. This catalytic system is applicable to gram-scale syntheses and demonstrates compatibility with various functional groups, including fluorine, chlorine, bromine, trifluoromethyl, and hydroxyl. Deuterium labeling experiments show that the BH3 counterpart of NH3•BH3 served as the hydride source, while the NH3 counterpart of ammonia borane acted as a proton source. It offers a novel approach for the preparation of partially saturated heterocyclic derivatives.

Key words: reduction, magnesium, indoles, quinoxalines, ammonia borane