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- W2953139356 abstract "Pd-catalyzed cross-coupling of furfural tosylhydrazones with aryl halides produces 2-furylmethylenepalladium halides, which can undergo intramolecular nucleophilic dearomatization to provide spiroacetal enol ethers. This is the first report on the formation of 2-furylmethylenepalladium halides from stable furfural hydrazones instead of from 2-furylmethyl halides, which are not readily accessible or are unstable." @default.
- W2953139356 created "2019-06-27" @default.
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- W2953139356 date "2014-12-04" @default.
- W2953139356 modified "2023-09-27" @default.
- W2953139356 title "ChemInform Abstract: Practical Access to Spiroacetal Enol Ethers via Nucleophilic Dearomatization of 2-Furylmethylenepalladium Halides Generated by Pd-Catalyzed Coupling of Furfural Tosylhydrazones with Aryl Halides." @default.
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- W2953139356 doi "https://doi.org/10.1002/chin.201451073" @default.
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