Jump to main content
Jump to site search

Issue 16, 2010
Previous Article Next Article

Asymmetric synthesis of bis-tetrahydrofuran cores in annonaceous acetogenins

Author affiliations

Abstract

The bis-THF cores of annonaceous acetogenins were synthesized using (3R,4R)-1,5-hexadiene-3,4-diol (1) as the sole source of carbon atoms. The methylene acetal function was applied as a new linker/tether to facilitate the ring-closing metathesis.

Graphical abstract: Asymmetric synthesis of bis-tetrahydrofuran cores in annonaceous acetogenins

Back to tab navigation

Supplementary files

Publication details

The article was received on 25 Mar 2010, accepted on 17 Jun 2010 and first published on 30 Jun 2010


Article type: Communication
DOI: 10.1039/C004672H
Org. Biomol. Chem., 2010,8, 3624-3626

  •   Request permissions

    Asymmetric synthesis of bis-tetrahydrofuran cores in annonaceous acetogenins

    C. Chen, T. Kuan, K. Lu and D. Hou, Org. Biomol. Chem., 2010, 8, 3624
    DOI: 10.1039/C004672H

Search articles by author

Spotlight

Advertisements