Highly Diastereoselective Synthesis of Substituted Pyrrolidines Using a Sequence of Azomethine Ylide Cycloaddition and Nucleophilic Cyclization-Reference-Cited by-同舟云学术

Highly Diastereoselective Synthesis of Substituted Pyrrolidines Using a Sequence of Azomethine Ylide Cycloaddition and Nucleophilic Cyclization

Published:2010-03-01 Issue:7 Volume:12 Page:1396-1399
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Bélanger Guillaume¹,Darsigny Véronique¹,Doré Michaël¹,Lévesque François¹

Affiliation:

1. Département de Chimie, Université de Sherbrooke, 2500 Boulevard Université, Sherbrooke, Québec J1K 2R1, Canada

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol902767b

Reference50 articles.

1. For a selection of reviews on the methods for the preparation of azomethine ylides and their 1,3-dipolar cycloadditions, see:

2. Intramolecular Dipolar Cycloaddition Reactions of Azomethine Ylides

3. bHarwood, L. M.; Vickers, R. J.InSynthetic Applications of 1.3-Dipolar Cyaloaddition Chemistry Toward Heterocycles and Natural Products;Padwa, A.; Pearson, W. H., Eds.Wiley:New York, 2003; pp169−252.

4. Ylides by the desilylation of .alpha.-silyl onium salts

5. For the gerenation of unstabilized azomethine ylides from demetalation of (trimethylsilyl)methyl- or (tributylstannyl)methyliminium ions, see ref1and:

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