Asymmetric Nucleophilic Additions Promoted by Quaternary Phosphonium Ion-Pair Catalysts

被引:8
|
作者
Chen, Lingzhu [1 ,2 ]
Deng, Youlin [1 ]
Li, Tingting [1 ]
Hu, Deyu [1 ]
Ren, Xiaoyu [2 ]
Wang, Tianli [2 ]
机构
[1] Guizhou Univ, Ctr R&D Fine Chem, Key Lab Green Pesticide & Agr Bioengn, State Key Lab Green Pesticide,Minist Educ, Guiyang 550025, Peoples R China
[2] Sichuan Univ, Coll Chem, Key Lab Green Chem & Technol, Minist Educ, Chengdu 610064, Peoples R China
来源
CCS CHEMISTRY | 2024年 / 6卷 / 09期
基金
中国国家自然科学基金;
关键词
quaternary phosphonium salts; ion-pair catalysts; asymmetric synthesis; organocatalysis; nucleophilic addition; PHASE-TRANSFER CATALYSTS; ENANTIOSELECTIVE MICHAEL ADDITION; DIRECT MANNICH REACTIONS; DIRECT HENRY REACTION; CONJUGATE ADDITION; CHIRAL PHOSPHINE; BRONSTED ACID; SALTS; IMINES; CONSTRUCTION;
D O I
10.31635/ccschem.024.202404039
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Chiral quaternary phosphonium ion -pair catalysis showcases a distinctive catalytic and stereoinductive mode arising from the synergy between ionic and noncovalent interactions. Over recent decades, this methodology has been widely adopted to facilitate enantioselective nucleophilic addition reactions, including conjugate addition, Henry reaction, Mannich reaction, Strecker reaction, and hydrophosphonylation. This strategy has been successfully applied to the synthesis of numerous structurally diverse and multifunctionalized molecules, featuring challenging stereogenic centers. This minireview specifically highlights the accomplishments in asymmetric nucleophilic addition facilitated by chiral quaternary phosphonium catalysts. Its purpose is to cultivate interest among researchers, encouraging more engagement in this field and establishing quaternary phosphonium ion -pair catalysis as a potent and dependable tool for synthetic and pharmaceutical chemists.
引用
收藏
页码:2110 / 2130
页数:21
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