Mannich reaction - Study guides, Class notes & Summaries

Organic chemistry,name reaction,mannich reaction and it's mechanism

Enol Enolates and Enamines: Enol Enolates: These are formed by deprotonating an alpha carbon adjacent to a carbonyl group in a molecule containing both a carbonyl and an enolizable proton. They are important intermediates in many organic reactions, particularly in aldol condensation and Claisen condensation reactions. Enamines: These are formed by the reaction of a secondary amine with a carbonyl compound, resulting in the formation of a carbon-nitrogen double bond. Enamines are versatile ...

Brief overview of reactions and mechanisms described in chapter 21.

Summary of S3 - Catalytic Asymmetric Reactions 1. Introduction 2. Organocatalytic aldol reactions 3. Asymmetric Mannich, oxygenation and amination reactions 4. Other organocatalytic enamine reactions 5. Organocatalytic radical reactions 6. Asymmetric iminium ion catalysis 7. Catalytic asymmetric cycloaddition reactions 8. Asymmetric nucleophilic addition to aldehydes