Structure of grignard reagents and organolithium compounds
โ Scribed by Gideon Fraenkel; David G. Adams; James Williams
- Book ID
- 104241906
- Publisher
- Elsevier Science
- Year
- 1963
- Tongue
- French
- Weight
- 279 KB
- Volume
- 4
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
โฆ Synopsis
several problems concerning the structure of kignard reagent: and organolithium compounds have been studied with the aid of nuclear magnetic resonance spectroscopy, NM&; they are: the ionic character of the carbon metal bonds, the rates of carbanion inversion, the rates of carbon metal exchange and the electron hybridization in the C-H bond in RCHM.
๐ SIMILAR VOLUMES
The title reaction afforded selenophilic, carbophilic, and reduction products depending on the kinds of the organometallic reagents and the heterophilic nature of the reaction was more conspicuous in the reaction with the selenoketone than with the corresponding thioketone.
dence for the rearrangement (2)+( 7). However, this isomerization can also be detected when (la) is used as starting material: Thus, on reaction of (la) with 6 equivalents of potassium tert-butoxide in THF at 35"C, the enol ether (10) is obtained in 44% yield. Its formation can be explained in terms