Chiral N,N′-dioxide ligands: synthesis, coordination chemistry and asymmetric catalysis

被引:339
|
作者
Liu, Xiaohua [1 ]
Lin, Lili [1 ]
Feng, Xiaoming [1 ]
机构
[1] Sichuan Univ, Coll Chem, Minist Educ, Key Lab Green Chem & Technol, Chengdu 610064, Peoples R China
来源
ORGANIC CHEMISTRY FRONTIERS | 2014年 / 1卷 / 03期
基金
中国国家自然科学基金;
关键词
UNPROTECTED 3-SUBSTITUTED OXINDOLES; HIGHLY EFFICIENT SYNTHESIS; ALPHA-DIAZOESTERS; KETONES; CYANOSILYLATION; COMPLEXES; SYMMETRY;
D O I
10.1039/c3qo00059a
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A class of conformationally flexible ligands composed of a tertiary amino oxide-amide backbone and a straight-chain alkyl spacer was developed. These C-2-symmetric chiral N,N'-dioxide ligands could be straightforwardly synthesized from readily available amino acids and amines. They act as neutral tetra-dentate ligands to bind a wide variety of metal ions. Non-planar cis-alpha M(N,N'-dioxide) complexes enable an intriguing and easily fine-tuned chiral platform for a number of asymmetric reactions. Privileged N,N'-dioxide ligands frequently show wide substrate generality and exceptional levels of stereocontrol for a specific catalytic reaction. We describe approaches to the ligand design and synthesis, structure and bonding in coordination complexes, and the recent developments in asymmetric catalysis.
引用
收藏
页码:298 / 302
页数:5
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