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ChemInform Abstract: Total Synthesis of Maturinone Through a Regioselective Diels-Alder Reaction of 5-Brominated Benzofurandione.

✍ Scribed by O. CHERKAOUI; P. NEBOIS; H. FILLION

Publisher: John Wiley and Sons
Year: 2010
Weight: 29 KB
Volume: 28
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.199738277

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✦ Synopsis

Total Synthesis of Maturinone Through a Regioselective Diels-Alder Reaction of 5-Brominated Benzofurandione.

-Using a known directing effect of a bromine atom located on the double bond of a quinone such as (III) in a Diels-Alder reaction maturinone ( VI) is synthesized in an efficient and regioselective way.

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