Alkylation and arylation of 2-trimethylsiloxyallyl halides with lithium dialkyl-and diarylcuprate, respectively, gave silyl enol ethers in a regiospecific manner.
A novel route to 2-carbamoylcycloalkanones by the addition reaction of silyl enol ethers to isocyanates
β Scribed by Iwao Ojima; Shinichi Inaba; Yoichiro Nagai
- Publisher
- Elsevier Science
- Year
- 1973
- Tongue
- French
- Weight
- 110 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
Silyl enol ethers are currently much interested in respect to the reaction of enolate anion, and many reports have been made on the formation and spectra of these compounds.
1 Little has been known, however, about the reactivity on the @-carbon of these compounds except trimethylsilylacetals. 2 We have found
π SIMILAR VOLUMES
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
Swrunary: ChromyZ chloride reacts regiospecifically with 0-silylated enolates to form cc-hydroxy ketones.