Formal Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Ylides to (S)-2-p-Tolylsulfinyl-2-cyclopentenone-Reference-Cited by-同舟云学术

Formal Asymmetric 1,3-Dipolar Cycloaddition of Azomethine Ylides to (S)-2-p-Tolylsulfinyl-2-cyclopentenone

Published:2003-11-22 Issue:26 Volume:68 Page:10013-10019
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, Cantoblanco, 28049 Madrid, Spain

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo035369w

Reference26 articles.

1. Asymmetric 1,3-Dipolar Cycloaddition Reactions

2. García Ruano, J. L.; Cid, B. InTopics in Current Chemistry; Page, P. C. B., Ed.; Springer: Berlin, 1999; Vol. 204, pp 1−126 (and references therein).

3. García Ruano, J. L.; Bercial, F.; González, G.; Martín Castro, A. M.; Martín, M. R.Tetrahedron: Asymmetry2002,13, 1993. (b) García Ruano, J. L.; Fraile, A.; Martín, M. R.Tetrahedron: Asymmetry1996,7, 1943. (c) García Ruano, J. L.; Fraile, A.; González, G.; Martín, M. R.; Clemente, F. R.; Gordillo, R. J. Org. Chem.2003,68, 6522.

4. 1,3-cycloaddition of nitrile oxides to cyclic and open-chain 4-oxo-2-sulfinylbut-2-enoic acid derivatives

5. 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

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