Chinese Journal of Organic Chemistry ›› 2020, Vol. 40 ›› Issue (5): 1129-1149.DOI: 10.6023/cjoc201911011 Previous Articles     Next Articles


王伟, 胡燚, 林睿褀, 吴恒, 童启, 汪连生, 肖祖峰, 朱磊   

  1. 湖北工程学院化学与材料科学学院 湖北孝感 432000
  • 收稿日期:2019-11-06 修回日期:2019-12-11 发布日期:2020-01-21
  • 通讯作者: 肖祖峰, 朱磊;
  • 基金资助:

Progress on the Synthesis of 1,3-Amino Alcohol

Wang Wei, Hu Yi, Lin Ruiqi, Wu Heng, Tong Qi, Wang Liansheng, Xiao Zufeng, Zhu Lei   

  1. School of Chemistry and Material Science, Hubei Engineering University, Xiaogan, Hubei 432000
  • Received:2019-11-06 Revised:2019-12-11 Published:2020-01-21
  • Supported by:
    Project supported by the Hubei Provincial Education Department Young and Middle-aged Talents Project (No. Q20172705), the National Natural Science Foundation of China (No. 21774029), and the Hubei University Excellent Young and Middle-aged Science and Technology Innovation Team Project (No. T201816).

Optically pure 1,3-amino alcohol is not only the important synthon in organic synthesis, but also the core structure of numerous bioactive molecule. As a result, the formation of 1,3-amino alcohols occupies a hot resarch topic in asymmetric synthesis. This review symmarizes several types of frequently-used methods and progress on synthesizing 1,3-amino alcohols:aldol or azo-aldol condensation synthesis, transition metal catalyzed C-H activation and amination synthesis, ring-opening and addition of azocyclic compounds, and[3+2] dipolar-cycloaddition reaction etc.

Key words: 1,3-amino alcohol, asymmetric synthesis, catalyst