The enantioselective total synthesis of(-)-myltaylenol

Sven Doye; Torsten Hotopp; Ekkehard Winterfeldt

doi:10.1039/A703164E

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The enantioselective total synthesis of (-)-myltaylenol

Sven Doye, Torsten Hotopp and Ekkehard Winterfeldt

Abstract

Using an intramolecular Diels–Alder cycloaddition followed by an oxidative rupture of the connective unit as the key step, the unusual carbon framework of (-)-myltaylenol was established.

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DOI: https://doi.org/10.1039/A703164E
Article type: Paper

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Chem. Commun., 1997, 1491-1492

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The enantioselective total synthesis of (-)-myltaylenol

S. Doye, T. Hotopp and E. Winterfeldt, Chem. Commun., 1997, 1491 DOI: 10.1039/A703164E

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Chemical Communications

The enantioselective total synthesis of (-)-myltaylenol

Abstract

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The enantioselective total synthesis of (-)-myltaylenol

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