Acta Chim. Sinica ›› 2019, Vol. 77 ›› Issue (3): 213-230.DOI: 10.6023/A18110470 Previous Articles     Next Articles

Review

手性高价碘试剂的发展及展望

蔡倩, 马浩文   

  1. 暨南大学药学院 广州 510530
  • 投稿日期:2018-11-21 发布日期:2019-01-28
  • 通讯作者: 蔡倩 E-mail:caiqian@jnu.edu.cn
  • 作者简介:蔡倩,暨南大学药学院研究员.2001年本科毕业于南开大学,2006年从上海有机所获博士学位,之后在密歇根大学癌症研究中心从事博士后研究,2009年加入中科院广州生物医药与健康研究院,2010年担任课题组长,2016年加入暨南大学药学院.蔡倩课题组研究兴趣集中在基于药物活性分子合成的新型串联反应以及不对称反应方法学研究及应用;马浩文,1996年生于湖北省黄石市,2018年本科毕业于山西医科大学药学院,现为暨南大学药学院药物化学专业硕士研究生,主要研究课题为高价碘促进的不对称反应.
  • 基金资助:

    项目受国家自然科学基金(Nos.21772066,21572229)以及广东省"特支"计划(No.2017TX04R059)资助.

Recent Advances of Chiral Hypervalent Iodine Reagents

Cai Qian, Ma Haowen   

  1. College of Pharmacy, Jinan University, Guangzhou 510530
  • Received:2018-11-21 Published:2019-01-28
  • Supported by:

    Project supported by the National Natural Science Foundation of China (Nos. 21772066, 21572229) and Guangdong Special Support Program (No. 2017TX04R059).

Hypervalent iodine chemistry has arose as an important field in organic chemistry in the past decades. Hypervalent iodine compounds, with reactivities similarly to transition metals in many different types of transformations, have attracted broad interests in organic community due to their practical advantages in the mild conditions, low costs, environmental benign and low toxicity. Great progresses have been made in this field. Chiral hypervalent iodine reagents or precursors have also been developed and utilized in a variety of asymmetric reactions in a stoichiometric or catalytic way. Important advances have been witnessed in the field of chiral hypervalent iodine chemistry in recent years. However, great limitations still exist. In this review, we have made a summary of different types of chiral hypervalent iodine reagents and precursors according to the characteristics of these compounds and the timeline. It may be helpful for the researchers to better understand the development and limitations of chiral hypervalent iodine chemistry.

Key words: chirality, chiral hypervalent iodine, chiral aryl iodide, asymmetric reaction, catalytic asymmetric synthesis