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Issue 3, 2003
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Enantioselective total synthesis of (−)-heliannuol A

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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

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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, 350-351
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    Enantioselective total synthesis of (−)-heliannuol A

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

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