Design and synthesis of new alkyl-based chiral phosphoric acid catalysts

被引:2
|
作者
Tang, Xiaoxue [1 ]
He, Hualing [1 ]
Fang, Xiantao [1 ]
Chang, Zexu [1 ]
Antilla, Jon C. [1 ]
机构
[1] Tianjin Univ, Inst Mol Design & Synth, Sch Pharmaceut Sci & Technol, Hlth Sci Platform, Tianjin 300072, Peoples R China
关键词
aliphatic substituents; asymmetric catalysis; BINOL; chiral phosphoric acids; organocatalysts; BRONSTED ACID; ALKENES; DESYMMETRIZATION; DERIVATIVES; ALLYLATION; ACTIVATION; LIGANDS; KETONES; VAPOL;
D O I
10.1002/chir.23101
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Using chiral BINOL-derived phosphoric acids (PA's) to activate substrates for enhanced reactivity is now regarded as a powerful strategy to control enantioselectivity in asymmetric synthesis. Generally, most substituents at the 3,3 '-positions of BINOL PA's are aryl derivatives. These derivatives are pivotal in attaining high selectivity. PA's with alkyl substituents in these positions have rarely been reported. Herein, we introduced alkyl-based substituents at the 3,3 '-position of PA's. These new potential catalysts, if applied in reactions, may allow altered noncovalent interactions (as opposed to the typical aryl substituents in these positions) with substrates used in chiral PA-catalyzed chemistry in the future.
引用
收藏
页码:592 / 602
页数:11
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