Synthesis of the Tetracyclic Core of the Neomangicols Using a Late-Stage Indene Alkylation-Reference-Cited by-同舟云学术

Synthesis of the Tetracyclic Core of the Neomangicols Using a Late-Stage Indene Alkylation

Published:2009-06-15 Issue:14 Volume:11 Page:3128-3131
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Wood Jessica L.¹,Pujanauski Brian G.¹,Sarpong Richmond¹

Affiliation:

1. Department of Chemistry, University of California, Berkeley, California 94720

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol9010008

Reference23 articles.

1. For a recent discussion on terpene synthesis, see:Hudlicky, T.; Reed, J.The Way of Synthesis: Evolution of Design and Methods for Natural Products Synthesis,1st ed.Wiley-VCH:Weinheim, 2007; pp207−215.

2. Neomangicols: Structures and Absolute Stereochemistries of Unprecedented Halogenated Sesterterpenes from a Marine Fungus of the Genus Fusarium

3. Enantioselective Synthesis of the Spirotetracyclic Carbon Core of Mangicols by Using a Stereoselective Transannular Diels–Alder Strategy

4. Evaluation of possible intramolecular [4+2] cycloaddition routes for assembling the central tetracyclic core of the potent marine antiinflammatory agent mangicol A

5. Exploration of conjugate addition routes to advanced tricyclic components of mangicol A

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