Synthesis of β,γ-disubstituted-γ-lactones through a Johnson–Claisen rearrangement: a short route to xylobovide, nor-canadensolide, canadensolide, sporothriolide and santolinolide-Reference-Cited by-同舟云学术

Synthesis of β,γ-disubstituted-γ-lactones through a Johnson–Claisen rearrangement: a short route to xylobovide, nor-canadensolide, canadensolide, sporothriolide and santolinolide

Published:2009-12 Issue:24 Volume:20 Page:2835-2844
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Fernandes Rodney A.,Ingle Arun B.,Chavan Vijay P.

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference45 articles.

1. Cytochalasins and phytotoxins from the fungus Xylaria obovata

2. Canadensolide - an antifungal metabolite of penicillium canadense

3. Biologically active metabolites from fungi. 3. Sporothriolide, discosiolide, and 4-epi-ethisolide New furofurandiones from Sporothrix sp., Discosia sp., and Pezicula livida.

4. Santolinolide B [(2R,3S,4S)-4-hydroxy-2,5-dimethyl-3-vinyl-5-hexenoic acid lactone]. A new irregular monoterpene from Artemisia tridentata tridentata

5. Synthesis of (±)-canadensolide and its C-5 epimer. Revision of the stereochemistry

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