Chiral Phosphoric Acids as Versatile Catalysts for Enantioselective Transformations

被引:841
作者
Terada, Masahiro [1 ]
机构
[1] Tohoku Univ, Dept Chem, Grad Sch Sci, Sendai, Miyagi 9808578, Japan
来源
SYNTHESIS-STUTTGART | 2010年 / 12期
关键词
asymmetric catalysis; diastereoselectivity; electrophilic addition; enantioselectivity; multicomponent reaction; FRIEDEL-CRAFTS ALKYLATION; DIELS-ALDER REACTIONS; MANNICH-TYPE REACTION; 1,3-DIPOLAR CYCLOADDITION REACTIONS; ASYMMETRIC TRANSFER HYDROGENATION; CARBONYL-ENE REACTION; N-BOC-IMINES; ORGANOCATALYTIC TRANSFER HYDROGENATION; BAEYER-VILLIGER REACTION; BOND-FORMING REACTIONS;
D O I
10.1055/s-0029-1218801
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Chiral phosphoric acids derived from axially chiral biaryls and related chiral Bronsted acids have emerged as an attractive and widely applicable class of enantioselective organocatalysts for a variety of organic transformations. This review focuses on recent achievements in the development of enantioselective transformations using these axially chiral phosphoric acids and their analogues as chiral Bronsted acid catalysts. The contents are arranged according to the specific types of carbon-carbon bond-forming reactions, followed by carbon-heteroatom bond-forming reactions and functional group transformations, including reduction and oxidation. Further applications to combined phosphoric acid and metal complex catalytic systems and new aspects in the development of chiral Bronsted acid catalysts are also highlighted.
引用
收藏
页码:1929 / 1982
页数:54
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