Asymmetric 1,3-Dipolar Cycloaddition of N-Metalated Azomethine Ylides to Methyl (S)-2-(p-Tolylsulfinyl)acrylate. Synthesis of Optically Pure 2,4,5-Trisubstituted 2,5-Dihydro-1H-pyrroles-Reference-Cited by-同舟云学术

Asymmetric 1,3-Dipolar Cycloaddition of N-Metalated Azomethine Ylides to Methyl (S)-2-(p-Tolylsulfinyl)acrylate. Synthesis of Optically Pure 2,4,5-Trisubstituted 2,5-Dihydro-1H-pyrroles

Published:2002-01-16 Issue:3 Volume:67 Page:981-987
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

García Ruano José Luis¹,Tito Amelia¹,Peromingo M. Teresa¹

Affiliation:

1. Departamento de Química Orgánica, Universidad Autónoma de Madrid, Cantoblanco, 28049 Madrid, Spain

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo010797s

Reference37 articles.

1. Pyrrolizidine and Indolizidine Syntheses Involving 1,3-Dipolar Cycloadditions

2. Asymmetric 1,3-Dipolar Cycloaddition Reactions

3. (a) Tsuge, O.; Kanemasa, S. InAdvances in Heterocyclic Chemistry; Katritzky, A. R., Ed.; Academic Press: San Diego, CA, 1989; Vol. 45, pp 232−349.

4. (b) Lown, J. W. In1,3-Dipolar Cycloaddition Chemistry; Padwa, A., Ed.; Wiley: New York, 1984; Vol. 1, pp 653−732.

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