Generation of azolium dienolates as versatile nucleophilic synthons via N-heterocyclic carbene catalysis

被引:55
作者
Gao, Jian [1 ]
Feng, Jie [1 ]
Du, Ding [1 ]
机构
[1] China Pharmaceut Univ, Dept Chem, State Key Lab Nat Med, Nanjing 210009, Peoples R China
来源
ORGANIC CHEMISTRY FRONTIERS | 2021年 / 8卷 / 21期
基金
中国国家自然科学基金;
关键词
ALPHA; BETA-UNSATURATED ACYL CHLORIDES; ENANTIOSELECTIVE GAMMA-AMINATION; 4+2 ANNULATION; ASYMMETRIC-SYNTHESIS; KINETIC RESOLUTION; AZOMETHINE IMINES; CARBON ACTIVATION; COOPERATIVE CATALYSIS; PHOTOREDOX CATALYSIS; BETA-HYDROXYLATION;
D O I
10.1039/d1qo01127h
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
N-Heterocyclic carbene (NHC) organocatalysis has emerged as a powerful tool in the field of modern organic synthesis especially in asymmetric construction of various cyclic skeletons. As emerging NHC-bound nucleophilic intermediates, azolium dienolates have been widely investigated and applied in NHC-catalyzed transformations due to their unique reactivities and versatile structures. Particularly, four representative kinds of reactive azolium dienolates (I-IV) have been explored as versatile nucleophilic synthons via either alpha-functinalization or remote gamma-functionalization to achieve efficient construction of complex skeletons. Moreover, these NHC-bound intermediates had wide-ranging applications in asymmetric synthesis of diversely enantioenriched centrally chiral molecules. In this review, the recent advances in NHC-catalyzed generation of azolium dienolates from different precursors and their applications in the synthesis of various valuable molecules are summarized comprehensively.
引用
收藏
页码:6138 / 6166
页数:29
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