Hydroxyl-group-activated azomethine ylides in organocatalytic H-bond-assisted 1,3-dipolar cycloadditions and beyond

Author:

Przydacz Artur12345,Bojanowski Jan12345,Albrecht Anna12345ORCID,Albrecht Łukasz12345ORCID

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

Reference54 articles.

1. Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry toward Heterocycles and Natural Products , ed. A. Padwa and W. H. Pearson , John Wiley and Sons , Hoboken, NJ , 2003

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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