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- W2006702457 abstract "In the presence of bis(trifluoromethyl) disulfide, methylphenylsulfonium bis(methoxycarbonyl)methylid is readily attacked by a nucleophile (an alkyl sulfide or a pyridine) and the corresponding new ylid is produced. In the NMR spectrum of a mixture of an ylid, an alkyl sulfide, and a catalytic disulfide, a remarkable broadening in the signals of the α-hydrogen of the sulfide was observed. A mechanism is suggested, which involves a complex from the two reactants and the catalyst." @default.
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- W2006702457 date "1973-12-01" @default.
- W2006702457 modified "2023-09-25" @default.
- W2006702457 title "Mechanism of Transylidation of Stable Sulfonium Ylids with Alkyl Sulfides in the Presence of Catalytic Disulfides" @default.
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- W2006702457 doi "https://doi.org/10.1246/bcsj.46.3828" @default.
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