γ-Silyl Alkyl Halides, Alcohols, and Esters Thereof
✍ Scribed by J. P. Michael; C. B. de Koning
- Publisher
- John Wiley and Sons
- Year
- 2003
- Weight
- 52 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0931-7597
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📜 SIMILAR VOLUMES
The O-silylated dienolates of unsaturated ketones and esters can be alkylated using zinc bromide catalysis to give predominantly the y-alkylated carbonyl compounds. The substitution pattern of the substrate (11, favours, in certain cases, very high or complete y-selectivity.
Ababmck Mono-and d&substituted phosphinic acids have km synthesti in a one-pot reaction, by the adition of alkyl halides to silyl phosphoaites, w&r mild andflaibk conditions.
Xn this communication we report the first example of a Claisen rearrangement involving an enamine as the ally1 double bond and a general, high yield synthesis of silyl allenes.