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- W2006163911 abstract "Treatment of 4-substituted benzyldimethyl(triphenylsilylmethyl)ammonium halides (A) with lithium aluminum hydride afforded a high yield of triphenylsilane and an ammonium ylide intermediate, which was immediately converted into 5-substituted 2-methylbenzyldimethylamines (Sommelet—Hauser rearrangement products), 2-(4-substituted-phenyl)ethyldimethylamines (Stevens rearrangement products), and 4-substituted benzyldimethylamine. Reductive cleavage of nitrogencarbon bonds of compounds A was a minor process." @default.
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- W2006163911 title "Formation of ammonium ylides by the cleavage of siliconcarbon bonds of triphenylsilylmethylammonium salts" @default.
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- W2006163911 doi "https://doi.org/10.1016/s0022-328x(00)82547-4" @default.
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