Organocatalytic Atroposelective Reactions of Alkynes

被引:0
|
作者
Zhang, Zhi-Xin [1 ]
Hu, Tian-Qi [1 ]
Ye, Long-Wu [1 ,2 ]
Zhou, Bo [1 ]
机构
[1] Xiamen Univ, Coll Chem & Chem Engn, Key Lab Chem Biol Fujian Prov, Xiamen 361005, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China
来源
SYNTHESIS-STUTTGART | 2024年 / 56卷 / 15期
关键词
organocatalysis; enantioselectivity; alkynes; axially chiral compounds; reaction mechanism; ENANTIOSELECTIVE SYNTHESIS; BRONSTED ACID; ASYMMETRIC-SYNTHESIS; C-C; CONSTRUCTION; ATROPISOMERS; CYCLOISOMERIZATION; HYDROARYLATION; CYCLOADDITION; CATALYSIS;
D O I
10.1055/a-2241-3571
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The atroposelective transformation of alkynes is an efficient protocol for the assembly of axially chiral compounds. Benefit from the rapid development of chiral organocatalysts, the organocatalytic atroposelective reactions of alkynes have been extensively studied during the past decades. An array of chiral catalysts, including chiral Bronsted acid catalysts, secondary amine catalysts, N-heterocyclic carbene (NHC) catalysts, thiourea catalysts and N-squaramide catalysts, were employed into the enantioselective reactions of different alkynes. This review summarizes the recent advances in organocatalytic atroposelective reactions of alkynes according to the types of alkyne substrates. The reaction mechanisms, mode of enantiocontrol, product diversity and applications are highlighted in this review. © 2023 Georg Thieme Verlag. All rights reserved.
引用
收藏
页码:2316 / 2328
页数:13
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