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- W1596317205 abstract "Protolysis and ketone addition reactions are reported for neophentylallyllithium in THF solvent. The yield of the trans-C8H16 olefin essentially constant for protolysis with the following active hydrogen compounds: water, tert-butanol, 1-hexyne, cyclopentadiene, fluorene, and triphenylmethane. The relative yields of the cis- and α-neopentallyl isomers apparently depend on the steric bulk as well as the strength of the acid. The degree of allylic rearrangement observed from a series of ketones also is a function of the size of the ketone." @default.
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- W1596317205 date "1973-05-01" @default.
- W1596317205 modified "2023-09-27" @default.
- W1596317205 title "Neopentylallithium" @default.
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- W1596317205 doi "https://doi.org/10.1016/s0022-328x(00)95143-x" @default.
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