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- W2016506013 abstract "In the absence of a reactive alkene, the Diels-Alder dimer of 2,6-dimethyl-6-hydroxycyclohexa-2,4-dienone rearranges at 160 °C to a new dimer via a reverse Diels-Alder reaction, two α-hydroxyketone rearrangements, two Micheal additions, and two aldol condensations. © 1997 Elsevier Science Ltd." @default.
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- W2016506013 date "1997-04-01" @default.
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- W2016506013 title "Thermal Rearrangement of the Diels-Alder Dimer of 2,6-Dimethyl-6-hydroxycyclohexa-2,4-dienone to a Pentacyclic Dimer" @default.
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- W2016506013 doi "https://doi.org/10.1016/s0040-4039(97)00368-7" @default.
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