Hydroxyl-group-activated azomethine ylides in organocatalytic H-bond-assisted 1,3-dipolar cycloadditions and beyond
Author:
Affiliation:
1. Institute of Organic Chemistry
2. Faculty of Chemistry
3. Lodz University of Technology
4. 90-924 Łódź
5. Poland
Abstract
The recent progress in organocatalytic H-bond-assisted 1,3-dipolar cycloadditions is described.
Funder
Narodowe Centrum Nauki
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2021/OB/D0OB02380A
Reference54 articles.
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2. Asymmetric 1,3-Dipolar Cycloaddition Reactions
3. Intramolecular Dipolar Cycloaddition Reactions of Azomethine Ylides
4. Construction of Enantiopure Pyrrolidine Ring System via Asymmetric [3+2]-Cycloaddition of Azomethine Ylides
5. Enantioselective Copper-Catalyzed 1,3-Dipolar Cycloadditions
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