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- W1996481191 abstract "A number of (E)-3-alkylidine-phthalide derivatives have been prepared at room temperature in excellent yields in a one-pot reaction by treating o-alkenylbenzoic acids with meta-chloroperbenzoic acid and para-toluenesulfonic acid. This reaction presumably occurs via domino epoxidation – intramolecular cyclization – acid catalyzed dehydration sequence of reactions. On the other hand, 3-(2-formyl-3,4-dihydro-naphthalen-1-yl)-acrylic acid esters and 3-(2-formyl-3,4-dihydro-naphthalen-1-yl)-acrylonitriles afforded phthalide derivatives under Pinnick reaction conditions involving oxidation-intramolecular Michael addition." @default.
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- W1996481191 date "2013-01-01" @default.
- W1996481191 modified "2023-10-07" @default.
- W1996481191 title "Synthesis of phthalides utilizing a one-pot intramolecular domino protocol" @default.
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- W1996481191 doi "https://doi.org/10.1039/c3ra45117h" @default.
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