<Abstract of Published Report>Synthesis of Phenylethynyldibenzoselenophenium Salt and Its Reactions with Nucleophiles
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- Reexamination of Products and the Reaction Mechanism of the Chalcogeno-Baylis-Hillman Reaction : Chalcogenide-TiCl_4-mediated Reactions of Electron-deficient Alkenes with Aldehydes.
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- Structure and Reaction of 2,6-Bis(alkoxycarbonyl)-1-methyl-2H-and 4H-Selenopyranium Tetrafluoroborates.
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- Structure and Reaction of 2,6-Bis(alkoxycarbonyl)-1-methyl-2H- and 4H-Selenopyranium Tetrafluoroborates
- A New Entry to Enantioselective Synthesis of α-Nethylene-β-hydroxy Ketones by the Chalcogeno-Baylis-Hillman Reaciton
- The Enantioselective Chalcogeno - Baylis - Hillman Reaction Using a Chiral Hydroxy Chalcogenide - TiCl_4 Complex
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- Novel Acylation of a Vinyl Group by the Reaction of an Aldehyde and a Vinylselenonium Ylide.
- Synthesis of Phenylethynyldibenzoselenophenium Salt and Its Reactions with Nucleophiles
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