Stereospecific Synthesis of Pyrrolidines with Varied Configurations via 1,3-Dipolar Cycloadditions to Sugar-Derived Enones-Reference-Cited by-同舟云学术

Stereospecific Synthesis of Pyrrolidines with Varied Configurations via 1,3-Dipolar Cycloadditions to Sugar-Derived Enones

Published:2014-05-23 Issue:11 Volume:79 Page:4992-5006
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Udry Guillermo A. Oliveira¹,Repetto Evangelina¹,Varela Oscar¹

Affiliation:

1. CIHIDECAR-CONICET-UBA, Departamento de Química Orgánica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Pabellón 2-Ciudad Universitaria, Buenos Aires 1428, Argentina

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo500547y

Reference61 articles.

1. Enantioselective Copper-Catalyzed 1,3-Dipolar Cycloadditions

2. Asymmetric 1,3-dipolar cycloadditions

3. Construction of Enantiopure Pyrrolidine Ring System via Asymmetric [3+2]-Cycloaddition of Azomethine Ylides

4. Intramolecular Dipolar Cycloaddition Reactions of Azomethine Ylides

5. Amaryllidaceae, Sceletium, imidazole, oxazole, thiazole, peptide and miscellaneous alkaloids (July 1998 to June 1999)

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