A Versatile Stereoselective Synthesis of endo,exo-Furofuranones: Application to the Enantioselective Synthesis of Furofuran Lignans-Reference-Cited by-同舟云学术

A Versatile Stereoselective Synthesis of endo,exo-Furofuranones: Application to the Enantioselective Synthesis of Furofuran Lignans

Published:2003-12-12 Issue:1 Volume:69 Page:122-129
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Swain Nigel A.¹,Brown Richard C. D.¹,Bruton Gordon¹

Affiliation:

1. Department of Chemistry, The University of Southampton, Highfield, Southampton SO17 1BJ, U.K., and GlaxoSmithKline Pharmaceuticals, New Frontiers Science Park, Harlow, Essex CM19 5AW, U.K.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo035365r

Reference38 articles.

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3. The Ca2+ antagonist activity of lignans.

4. New metabolites, tetrahydrofuran lignans, produced by Streptomyces sp. IT-44.

5. Inhibition of cyclic AMP phosphodiesterase by lignans.

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