Journal
JOURNAL OF ORGANIC CHEMISTRY
Volume 71, Issue 7, Pages 2802-2810Publisher
AMER CHEMICAL SOC
DOI: 10.1021/jo052609u
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Efficient total syntheses of the sponge-derived hydrocarbon polyacetylenes callyberynes A-C have been achieved using metal-catalyzed cross-coupling reactions of highly unsaturated 1,3-diyne fragments as the key steps, namely: Cadiot-Chodkiewicz reaction under Alamis optimized conditions (sp-sp), sequential Sonogashira reaction of a cis,cis-divinyl dihalide (sp(2)-sp), and Kumada-Corriu reaction of an unactivated alkyl iodide (sp(3)-sp). This last approach constitutes the first application of a metalcatalyzed sp(3)-sp Kumada-Corriu cross-coupling reaction to the synthesis of a natural product.
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