Reaction of lithio N,N-dimethyl-trimethylsilylacetamide with acylating reagents. A synthesis of β-enamino amides
✍ Scribed by Richard P. Woodbury; Michael W. Rathke
- Book ID
- 104237131
- Publisher
- Elsevier Science
- Year
- 1978
- Tongue
- French
- Weight
- 200 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
Lithio tert-butyl trimethylsilylacetate, 4, reacts with acyl imidazoles (X = 1 to give good yields of B-keto esters, presumably by elimination of tri-') methylsilylimidazole from intermediate 5.' However, attempts to react &
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## Abstract Stereoselective construction of trisubstituted alkenes has wide applicability to the synthesis of many natural products Specifically, β‐disubstituted enones are important functionalized trisubstituted alkene targets. The reaction of organocerium reagents with secondary β‐enamino ketones