[5 + 2] Pyrone−Alkene Cycloaddition Approach to Tetrahydrofurans. Expeditious Synthesis of (±)-Nemorensic Acid-Reference-Cited by-同舟云学术

[5 + 2] Pyrone−Alkene Cycloaddition Approach to Tetrahydrofurans. Expeditious Synthesis of (±)-Nemorensic Acid

Published:1999-05-26 Issue:12 Volume:64 Page:4560-4563
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Rodríguez J. Ramón¹,Rumbo Antonio¹,Castedo Luis¹,Mascareñas José L.¹

Affiliation:

1. Departamento de Química Orgánica y Unidad Asociada al CSIC, Universidad de Santiago de Compostela, 15706 Santiago de Compostela, Spain

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo990233c

Reference20 articles.

1. (a) Wender, P. A.; Miller, B. L. InOrganic Synthesis: Theory and Applications; Hudlicky, T., Ed.; Jai Press: 1993; Vol. 2, p 27.

2. (b) Bertz, S. H.; Sommer, T. J. InOrganic Syntheses: Theory and Applications; Hudlicky, T., Ed.; Jai Press: 1993; Vol. 2, p 67. See also: (c)Chem. Rev.1996,96, 1.

3. Temporary tethering strategies for [5 + 2] pyrone-alkene cycloadditions

4. A Practical Approach to cis-2,5-Disubstituted Tetrahydrofurans and O-Bridged Medium-Sized Carbocycles from [5 + 2] Pyrone−Alkene Cycloadducts

5. Straightforward Construction of Fused 6,7,5-Tricarbocyclic Systems by Tandem [5 + 2]/[4 + 2] Cycloadditions

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