Citation: Wang Cai, Zhou Feng, Zhou Jian. Recent Advances in the Enantioselective Copper(Ⅰ)-Catalyzed Azide-Alkyne Cycloaddition Reaction[J]. Chinese Journal of Organic Chemistry, ;2020, 40(10): 3065-3077. doi: 10.6023/cjoc202005020 shu

Recent Advances in the Enantioselective Copper(Ⅰ)-Catalyzed Azide-Alkyne Cycloaddition Reaction

Wang Cai ^a ,
Zhou Feng ^a,, ,
Zhou Jian ^a,b,,

a.
Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai 200062
b.
State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032

Corresponding author: Zhou Feng, fzhou@chem.ecnu.edu.cn Zhou Jian, jzhou@chem.ecnu.edu.cn
Received Date: 9 May 2020
Revised Date: 28 May 2020
Available Online: 8 June 2020
Fund Project: the National Natural Science Foundation of China 21871090the National Natural Science Foundation of China 21672068Project supported by the National Natural Science Foundation of China (Nos. 21672068, 21871090)

Figures(17)

As one of the most important click reactions, the copper-catalyzed azide-alkyne cycloaddition (CuAAC) has found widespread applications. Nevertheless, the exploitation of enantioselective CuAAC remains largely undeveloped. Although the reaction itself does not generate chiral elements, the enantioselective CuAAC can be realized via the desymmetrization of prochiral dialkynes or diazides, as well as the kinetic resolution of racemic azides or terminal alkynes. Notably, enantioselective CuAAC provides efficient access to structurally diverse enantioenriched compounds featuring an azide, terminal alkyne or 1, 4-disubstituted 1, 2, 3-triazoles, which are valuable structural units in organic synthesis or medicinal chemistry. Since the first highly enantioselective CuAAC reaction via desymmetrization of prochiral diynes was reported in 2013, substantial progress has been made in this research area. To date, enantioselective CuAAC has been successfully applied to the construction of central chirality, axial chirality and planar chirality. The recent exciting achievements are summarized, the challenges in this context are briefly discussed, and the synthetic opportunities for future development are outlined.
- copper-catalyzed azide-alkyne cycloaddition (CuAAC) reaction,
- desymmetrization,
- (dynamic) kinetic resolution
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