Brønsted Acid-Catalyzed Three-Component 1,3-Dipolar Cycloadditions of 1,2-Disubstituted Alkynes with Aldehyde-Generated Azomethine Ylides
Author:
Affiliation:
1. School of Chemistry & Chemical Engineering, and Jiangsu Key Laboratory of Green Synthetic Chemistry for Functional Materials; Jiangsu Normal University; Xuzhou 221116 China
Publisher
Wiley
Subject
Organic Chemistry
Reference60 articles.
1. Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry Toward Heterocycles and Natural Products
2. Enantiospecific Synthesis of Heterocycles from α-Amino Acids
3. Intramolecular Dipolar Cycloaddition Reactions of Azomethine Ylides
4. Construction of Enantiopure Pyrrolidine Ring System via Asymmetric [3+2]-Cycloaddition of Azomethine Ylides
5. Intramolecular 1,3-dipolar cycloaddition reactions in targeted syntheses
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1. Protecting Group-Dependent Synthesis of Densely Substituted Dihydropyrroles v/s Pyrroles via 5-Exo-trig Cascade Radical Cyclization to Alkynyl Vinylogous Carbamates;The Journal of Organic Chemistry;2022-05-11
2. Addition Reactions: Cycloaddition;Organic Reaction Mechanisms Series;2019-03-07
3. 1,3-Dipolar cycloaddition reactions of azomethine ylides and alkynes;Chemistry of Heterocyclic Compounds;2018-12
4. ChemInform Abstract: Broensted Acid-Catalyzed Three-Component 1,3-Dipolar Cycloadditions of 1,2-Disubstituted Alkynes with Aldehyde-Generated Azomethine Ylides;ChemInform;2015-11-19
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