4.7 Article

Enantioselective total synthesis of (-)-heliannuol A

Journal

CHEMICAL COMMUNICATIONS
Volume -, Issue 3, Pages 350-351

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/b211227b

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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.

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