2022Unpublished venueRequires access

ASYMMETRIC ACID ORGANOCATALYSIS

Takahiko Akiyama

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Abstract

Chiral acid organocatalysts including hydrogen bond catalysts and chiral Brønsted acids surged after 2000. Recent progress in the chiral Brønsted acid catalysis mainly after 2010 is discussed, focusing on relatively stronger Brønsted acids such as chiral phosphoric acid derived from binaphthol, and their analogues. Transformation mediated by chiral Brønsted acid is organized by the type of reactions: nucleophilic reaction, cycloaddition reaction, Michael addition reaction, reduction, addition to alkenes, substitution, rearrangement, and others.

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What this paper is about

Chiral acid organocatalysts including hydrogen bond catalysts and chiral Brønsted acids surged after 2000. Recent progress in the chiral Brønsted acid catalysis mainly after 2010 is discussed, focusing on relatively stronger Brønsted acids such as chiral phosphoric acid derived from binaphthol, and their analogues. Transformation mediated by chiral Brønsted acid is organized by the type of reactions: nucleophilic reaction, cycloaddition reaction, Michael addition reaction, reduction, addition to alkenes, substitution, rearrangement, and others.

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Available abstract

Chiral acid organocatalysts including hydrogen bond catalysts and chiral Brønsted acids surged after 2000. Recent progress in the chiral Brønsted acid catalysis mainly after 2010 is discussed, focusing on relatively stronger Brønsted acids such as chiral phosphoric acid derived from binaphthol, and their analogues. Transformation mediated by chiral Brønsted acid is organized by the type of reactions: nucleophilic reaction, cycloaddition reaction, Michael addition reaction, reduction, addition to alkenes, substitution, rearrangement, and others.

Key concepts: Brønsted–Lowry acid–base theory, Organocatalysis, Phosphoric acid, Chemistry, Catalysis, Nucleophile, Cycloaddition, Organic chemistry

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