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- W2163053487 abstract "A series of 3,4-disubstituted α-methylene-γ-lactones were synthesized by the addition reaction of allylic bromide with aldehyde via sonochemical Barbier-type reaction condition and then followed by the in situ intramolecular esterification. The α-methylene-γ-lactone was produced as the sole product when THF/PhH solvent mixture was used whereas the allylation adduct was generated as the major product when solvent DMF was used." @default.
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- W2163053487 date "2002-11-01" @default.
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- W2163053487 title "Synthesis of 3,4-disubstituted α-methylene-γ-lactones via sonochemical Barbier-type reaction" @default.
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- W2163053487 doi "https://doi.org/10.1016/s0040-4039(02)02088-9" @default.
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