An improved synthesis of 2-substituted-3-furoic acids leading to an intramolecular Diels–Alder reaction between a dienophile and furan diene both containing an electron withdrawing group-Reference-Cited by-同舟云学术

An improved synthesis of 2-substituted-3-furoic acids leading to an intramolecular Diels–Alder reaction between a dienophile and furan diene both containing an electron withdrawing group

Published:1992 Issue:21 Volume: Page:2729-2731
ISSN:0300-922X
Container-title:J. Chem. Soc., Perkin Trans. 1
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Yu Shuyuan,Beese Giovanna,Keay Brian A.

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1992/P1/P19920002729

Reference49 articles.

1. Avarol a novel sesquiterpenoid hydroquinone with a rearranged drimane skeleton from the sponge

2. The absolute configuration of avarol, a rearranged sesquiterpenoid hydroquinone from a marine sponge

3. Metabolites of the Palauan sponge dactylospongia sp.

4. A New Bioactive Derivative of Avarol from the Marine Sponge Dysidea avara

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