4.5 Review

Chiral Phosphoric Acids as Versatile Catalysts for Enantioselective Transformations

Journal

SYNTHESIS-STUTTGART
Volume -, Issue 12, Pages 1929-1982

Publisher

GEORG THIEME VERLAG KG
DOI: 10.1055/s-0029-1218801

Keywords

asymmetric catalysis; diastereoselectivity; electrophilic addition; enantioselectivity; multicomponent reaction

Funding

  1. Ministry of Education, Culture, Sports, and Science and Technology, Japan

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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.

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