Jump to main content
Jump to site search

Issue 3, 2003
Previous Article Next Article

Enantioselective total synthesis of (−)-heliannuol A

Author affiliations


An efficient and enantiocontrolled total synthesis of (−)-heliannuol A has been accomplished by employing ring closing metathesis and sequential diastereoselective epoxidation and regioselective reductive cleavage of the epoxide ring.

Graphical abstract: Enantioselective total synthesis of (−)-heliannuol A

Back to tab navigation

Publication details

The article was received on 14 Nov 2002, accepted on 16 Dec 2002 and first published on 09 Jan 2003

Article type: Communication
DOI: 10.1039/B211227B
Citation: Chem. Commun., 2003,0, 350-351

  •   Request permissions

    Enantioselective total synthesis of (−)-heliannuol A

    H. Kishuku, M. Shindo and K. Shishido, Chem. Commun., 2003, 0, 350
    DOI: 10.1039/B211227B

Search articles by author