Recent developments in the total synthesis of natural products using the Ugi multicomponent reactions as the key strategy
Author:
Affiliation:
1. Instituto de Química Rosario (IQUIR, CONICET-UNR) and Facultad de Ciencias Bioquímicas y Farmacéuticas – Universidad Nacional de Rosario, Suipacha 531 (2000), Rosario, Argentina
Abstract
Funder
Consejo Nacional de Investigaciones Científicas y Técnicas
Fondo para la Investigación Científica y Tecnológica
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2024/OB/D3OB01837G
Reference391 articles.
1. Natural Products as Sources of New Drugs over the Nearly Four Decades from 01/1981 to 09/2019
2. Bridging the gap between natural product synthesis and drug discovery
3. Modularity: Adding New Dimensions to Total Synthesis
4. Inspirations, Discoveries, and Future Perspectives in Total Synthesis
5. Perspectives from nearly five decades of total synthesis of natural products and their analogues for biology and medicine
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2. Relevant Developments in the Use of Three‐Component Reactions for the Total Synthesis of Natural Products. The last 15 Years;ChemistryOpen;2024-04-22
3. Diastereoselective Synthesis of High Functionalized 4‐Imidazolidinone‐Tetrahydro‐β‐Carboline Hybrids via Divergent Post‐Ugi Transformation;Advanced Synthesis & Catalysis;2024-04-16
4. Review of application of the I2 and dimethyl sulfoxide combined reagent system to aryl methyl ketones for diverse transformations;Organic Chemistry Frontiers;2024
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