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- W4239967987 abstract "Abstract The preparation of an organic lithium reagent by reductive lithiation of an alkyl or aryl thioether with an aromatic radical anion (e.g., lithium naphthalene) in THF is generally referred to as the Screttas lithiation. It has been noticed that the less stable the organic lithium is, the greater the ease of generating the organic lithium by reductive lithiation. The resulting lithium reagent can react with a variety of electrophiles and shows high stereoselectivity. The study finds that the generated lithium species also undergoes an intramolecular cyclization. This reaction is useful for various applications in carbanion chemistry." @default.
- W4239967987 created "2022-05-12" @default.
- W4239967987 date "2010-09-15" @default.
- W4239967987 modified "2023-10-16" @default.
- W4239967987 title "Screttas Lithiation" @default.
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- W4239967987 doi "https://doi.org/10.1002/9780470638859.conrr575" @default.
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