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- W2023682784 abstract "Optically active trialkylsilyllithiums, (R)-(n-butyl)methylphenylsilyllithium (63% ee) and (S)-methyl(1-naphthyl)phenylsilyllithium (96% ee), were prepared by cleavage of the siliconsilicon bond of (R)-1-(n-butyl)-1-methyl-1-phenyl-2,2-diphenyl-2-methyldisilane with lithium metal, or the silicontin bond of (S)-methyl(1-naphthyl)phenylsilyltrimethylstannane with methyllithium, respectively. Optical purity of the silyllithiums was evaluated as corresponding silanes by HPLC on optically active stationary phase after hydrolysis. The formation of silyllithium was found to be highly stereospecific (>94, >99% retention, respectively). (S)-Methyl(1-naphthyl)phenylsilyllithium is configurationally stable for at least 1 h at −78°C in tetrahydrofuran." @default.
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- W2023682784 date "2001-01-09" @default.
- W2023682784 modified "2023-09-27" @default.
- W2023682784 title "ChemInform Abstract: Stereospecific Formation of Optically Active Trialkylsilyllithiums and Their Configurational Stability." @default.
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- W2023682784 doi "https://doi.org/10.1002/chin.200102032" @default.
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