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- W2552350464 abstract "A dearomative reduction of simple arenes has been developed which employs a visible-light-mediated cycloaddition of arenes with an N-N-arenophile and in situ diimide reduction. Subsequent cycloreversion or fragmentation of the arenophile moiety affords 1,3-cyclohexadienes or 1,4-diaminocyclohex-2-enes, compounds that are not synthetically accessible using existing dearomatization reactions. Importantly, this strategy also provides numerous opportunities for further derivatization as well as site-selective functionalization of polynuclear arenes." @default.
- W2552350464 created "2016-11-30" @default.
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- W2552350464 date "2016-11-23" @default.
- W2552350464 modified "2023-10-18" @default.
- W2552350464 title "Arenophile-Mediated Dearomative Reduction" @default.
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- W2552350464 doi "https://doi.org/10.1002/anie.201609686" @default.
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