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• W2894963640 abstract "A unique approach toward the preparation of cyclohexenynone equivalents was successfully developed via oxidative dearomatization of aryne precursors, featuring multiple functionalities on the target rings. Upon activation, these in situ formed cyclohexenynone intermediates exhibit good to excellent reactivity with various trapping agents. Moreover, an unprecedented cascade was discovered with aryl allyl sulfoxides, revealing a deeper utilization of the alkyne bond by concomitantly introducing one nucleophile and two electrophiles." @default.
• W2894963640 created "2018-10-12" @default.
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• W2894963640 date "2018-10-04" @default.
• W2894963640 modified "2023-10-14" @default.
• W2894963640 title "Cyclohexenynone Precursors: Preparation via Oxidative Dearomatization Strategy and Reactivity" @default.
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• W2894963640 doi "https://doi.org/10.1021/jacs.8b08915" @default.
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• W2894963640 hasPublicationYear "2018" @default.
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