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Organocatalyzed Asymmetric α-Oxidation, α-Aminoxylation and α-Amination of Carbonyl Compounds

Journal

MOLECULES
Volume 15, Issue 2, Pages 917-958

Publisher

MDPI
DOI: 10.3390/molecules15020917

Keywords

organocatalyst; chiral catalyst; alpha-oxidation; alpha-amination; alpha-aminoxylation; nitrosoaldol reaction; aldehyde; ketone; active methylene compound

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Organocatalytic asymmetric alpha-oxidation and amination reactions of carbonyl compounds are highly useful synthetic methodologies, especially in generating chiral building blocks that previously have not been easily accessible by traditional methods. The concept is relatively new and therefore the list of new catalysts, oxidizing and aminating reagents, as well as new substrates, are expanding at an amazing rate. The scope of this review includes new reactions and catalysts, mechanistic aspects and synthetic applications of alpha-oxidation, hydroxylation, aminoxylation, amination, hydrazination, hydroxyamination and related alpha-heteroatom functionalization of aldehydes, ketones and related active methylene compounds published during 2005-2009.

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