A Review on Generation and Reactivity of the N-Heterocyclic Carbene-Bound Alkynyl Acyl Azolium Intermediates

被引:14
|
作者
Dong, Ziyang [1 ]
Jiang, Chengming [1 ]
Zhao, Changgui [1 ]
机构
[1] Beijing Normal Univ, Coll Chem, Key Lab Radiopharmaceut, Minist Educ, Beijing 100875, Peoples R China
来源
MOLECULES | 2022年 / 27卷 / 22期
基金
北京市自然科学基金; 中国国家自然科学基金;
关键词
N-heterocyclic carbene; alkynyl acyl azolium; annulation; intermediate; mechanism; FORMAL 3+3 ANNULATION; ENANTIOSELECTIVE SYNTHESIS; LUMO ACTIVATION; CATALYSIS; ACCESS; ESTERS; ACIDS; INDOLIN-3-ONES; MECHANISM; ALPHA;
D O I
10.3390/molecules27227990
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
N-heterocyclic carbene (NHC) has been widely used as an organocatalyst for both umpolung and non-umpolung chemistry. Previous works mainly focus on species including Breslow intermediate, azolium enolate intermediate, homoenolate intermediate, alkenyl acyl azolium intermediate, etc. Notably, the NHC-bound alkynyl acyl azolium has emerged as an effective intermediate to access functionalized cyclic molecular skeleton until very recently. In this review, we summarized the generation and reactivity of the NHC-bound alkynyl acyl azolium intermediates, which covers the efforts and advances in the synthesis of achiral and axially chiral cyclic scaffolds via the NHC-bound alkynyl acyl azolium intermediates. In particular, the mechanism related to this intermediate is discussed in detail.
引用
收藏
页数:15
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