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• W1878373409 abstract "Abstract Allyl, dimethylallyl and prenyl ethers derived from o ‐acylphenols reacted upon microwave irradiation to form C ‐allylated or ‐prenylated chromone derivatives, depending on the substitution pattern of the arene and the allyl substituent. The reaction proceeds through a tandem Claisen rearrangement and 6‐ endo ‐ trig or 6‐ endo ‐ dig cyclization sequence. For prenyl ethers, the tandem sequence can be extended by a Cope rearrangement to furnish 6‐prenylchromones. The method is potentially useful for the synthesis of natural products and drugs." @default.
• W1878373409 created "2016-06-24" @default.
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• W1878373409 creator A5051658191 @default.
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• W1878373409 date "2015-10-29" @default.
• W1878373409 modified "2023-10-16" @default.
• W1878373409 title "Tandem Claisen Rearrangement/6-<i>endo</i>Cyclization Approach to Allylated and Pren­ylated Chromones" @default.
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• W1878373409 doi "https://doi.org/10.1002/ejoc.201501151" @default.
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