Molecules 2004, 9(6), 498-512; doi:10.3390/90600498

Synthesis of Pyran and Pyranone Natural Products

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Received: 25 March 2004; Accepted: 5 April 2004 / Published: 31 May 2004
(This article belongs to the Special Issue RACI 2003 symposium)
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract: An overview of the synthesis of the fungal metabolites (+)-dermolactone, (–)- semixanthomegnin, (+)- and (–)-mellein, (–)-ochratoxin α, (–)-(1R,3S)-thysanone, the enantiopure ventiloquinones L, E and G, and 8-desmethyleleutherin from a common chiral intermediate, is presented. Further methodology leading potentially toward extended quinones such as (3S,3'S)-xylindein is also outlined.
Keywords: Stereospecific synthesis; fungal metabolites; quinones; isochromanones.
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MDPI and ACS Style

Donner, C.D.; Gill, M.; Tewierik, L.M. Synthesis of Pyran and Pyranone Natural Products. Molecules 2004, 9, 498-512.

AMA Style

Donner CD, Gill M, Tewierik LM. Synthesis of Pyran and Pyranone Natural Products. Molecules. 2004; 9(6):498-512.

Chicago/Turabian Style

Donner, Christopher D.; Gill, Melvyn; Tewierik, Leonie M. 2004. "Synthesis of Pyran and Pyranone Natural Products." Molecules 9, no. 6: 498-512.

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