1963
DOI: 10.1016/s0040-4039(01)90713-0
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Structure of grignard reagents and organolithium compounds

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1963
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Cited by 31 publications
(3 citation statements)
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“…An equivalent amount of dioxane plus a 1% excess was slowly added to the Grignard and then stirred overnight. The ether was then replaced by THF by distillation according to the method of Storfer.6 15. Magnesium Bromide in THF.-1,2-Dibromoethane was added to magnesium turnings in THF using the high-vacuum system.…”
Section: Methodsmentioning
confidence: 99%
“…An equivalent amount of dioxane plus a 1% excess was slowly added to the Grignard and then stirred overnight. The ether was then replaced by THF by distillation according to the method of Storfer.6 15. Magnesium Bromide in THF.-1,2-Dibromoethane was added to magnesium turnings in THF using the high-vacuum system.…”
Section: Methodsmentioning
confidence: 99%
“…Main efforts in this field, initiated in the 1960s, consisted of registering 1 H, 13 C, 7 Li, , and then later on 6 Li magnetic resonance spectra of organolithium reactants in deuterated solvents. Compared with the crystallographic approach, the NMR technique is supposed to afford a more representative picture of the lithio reactant structure when engaged in a reaction, since the analyses are made in solution.…”
Section: Oligomaasmentioning
confidence: 99%
“…Although alkenyllithiums were the object of observations from the early 1960s, , a clear and precise description of their homoaggregation only began in the mid-1980s . Thus, vinyllithium crystallized with 1 equiv of tetrahydrofuran as a single tetrasolvated cubic tetramer of formula [VinylLi] 4 ·4THF (Scheme , left).…”
Section: Oligomaasmentioning
confidence: 99%