Enantioselective synthesis of monocerin and fusarentin ethers: Antifungal and insecticidal fungal metabolites.

Dillon, Michael P., Simpson, Thomas J. and Sweeney, Joseph B. (1992) Enantioselective synthesis of monocerin and fusarentin ethers: Antifungal and insecticidal fungal metabolites. Tetrahedron Letters, 33 (49). pp. 7569-7572. ISSN 0040-4039

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Abstract

Fusarentin 4,5-dimethyl ether (4) is synthesized via condensation of the benzylic anion of ethyl 3,4,5-trimethoxy-6-methylbenzoate (7) with (S)-3-tetrahydropyranyloxyhexanal (8); subsequent biomimetic cyclisation of (4) gives monocerin (1).

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URI:

https://eprints.hud.ac.uk/id/eprint/15417

URI:

https://eprints.hud.ac.uk/id/eprint/15417

URI:

https://eprints.hud.ac.uk/id/eprint/15417

Title:

Enantioselective synthesis of monocerin and fusarentin ethers: Antifungal and insecticidal fungal metabolites.

Creators:

Dillon, Michael P., Simpson, Thomas J. and Sweeney, Joseph B.

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