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- W1973061315 abstract "Reductive lithiation of 3,5-dimethoxybenzyl methyl ether was successfully performed with lithium wire and a catalytic amount of naphthalene in dry tetrahydrofuran at −15°C, leading to the quantitative generation of 3,5-dimethoxybenzyllithium. This organometallic compound, which can be stored for at least 24 h, was trapped with a variety of different electrophiles, including, besides aldehydes, non-functionalized and functionalized alkyl halides and an epoxide. Accordingly, it is a useful intermediate in the synthesis of 5-substituted natural and non-natural resorcinols. Copyright © 2003 John Wiley & Sons, Ltd." @default.
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- W1973061315 date "2003-01-01" @default.
- W1973061315 modified "2023-09-25" @default.
- W1973061315 title "Practical generation of 3,5-dimethoxybenzyllithium: application to the synthesis of 5-substituted-resorcinols" @default.
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- W1973061315 doi "https://doi.org/10.1002/aoc.531" @default.
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