Total synthesis of maturinone through a regioselective Diels-Alder reaction of 5-brominated benzofurandione

DOI: 10.1248/cpb.45.457

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 457 - 458 (1997)

Update date:2022-08-17

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Authors:

Cherkaoui, Omar

Nebois, Pascal

Fillion, Houda

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Article abstract of DOI:10.1248/cpb.45.457

Maturinone was efficiently prepared by means of a regiocontrolled Diels- Alder reaction between 5-bromo-2-ethoxycarbonyl-3-methylbenzo[b]furan-4,7- dione 8 and penta-1,3-diene.

Full text of DOI:10.1248/cpb.45.457

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Product name:3,5-Dimethylnaphtho[2,3-b]furan-4,9-dione

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