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- W2893703719 abstract "Methyl coumalate readily reacts with enamines at ambient temperature to give lactones, which can be further transformed into isophthalates and tetrahydronaphthoates. Both cyclic and acyclic enamines show good reactivity. Dehydrogenation of tetrahydronaphthoate 4a was achieved on a hundred-gram scale." @default.
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- W2893703719 date "2018-11-01" @default.
- W2893703719 modified "2023-09-24" @default.
- W2893703719 title "Divergent pathways to isophthalates and naphthalate esters from methyl coumalate" @default.
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- W2893703719 doi "https://doi.org/10.1016/j.tetlet.2018.09.058" @default.
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