Related Experiment Video
Updated: Jun 28, 2025

Versatile CO2 Transformations into Complex Products: A One-pot Two-step Strategy
Published on: November 9, 2019
Recent advances in the transformation reactions of the Betti base derivatives
Abolfazl Olyaei1, Mahdieh Sadeghpour2
1Department of Chemistry, Faculty of Science, Imam Khomeini International University Qazvin Iran Olyaei_a@sci.ikiu.ac.ir.
Abstract:
Betti bases are the products resulting from the one-pot multicomponent reaction involving 1-naphthol/2-naphthol, aliphatic/aromatic aldehydes, and secondary amines. This chemical process is commonly referred to as the Betti reaction. The significance of Betti bases in medicinal chemistry has grown substantially due to their diverse array of pharmacological applications. Furthermore, their synthetic utility is considerable, given their use as catalysts and ligands in asymmetric synthesis. Moreover, Mannich products, incorporating diverse functional groups such as -OH and -NH, find application in a range of organic reactions. This utilization enables the synthesis of novel C-C bond linkages and diverse heterocycles, including biologically active naphthoxazines, which hold biological applications such as antibacterial, antifungal and anticancer. The focus of this review article is on the application of aminonaphthol derivatives in transformation reactions and the synthesis of organic compounds, with particular emphasis on heterocycles.
More Related Videos
Related Concept Videos
Reactions of Aldehydes and Ketones: Baeyer–Villiger Oxidation
The carbonyl center is...
Factors Affecting α-Alkylation of Ketones: Choice of Base
The reaction involving bases like EtO− whose conjugate acid EtOH (pKa = 15.9) is stronger than the ketone (pKa = 19.2) results in an equilibrium mixture with higher ketone concentration. As a consequence,...
Diels–Alder Reaction Forming Bridged Bicyclic Products: Stereochemistry
E1 Reaction: Stereochemistry and Regiochemistry
Base-Promoted α-Halogenation of Aldehydes and Ketones
Cycloaddition Reactions: Overview

