Claisen rearrangement of ally1 vinyl ethers is an important general method of carboncarbon bond formation for synthesis of y,b-unsaturated aldehydes and ketones. 1 Syntheses of y,b-unsaturated esters and amides are similarly achieved by rearrangements of 2-alkoxy and 2amino-3-oxa-1,5-hexadienes.
β¦ LIBER β¦
Propargyloxy ketone enol ether-claisen rearrangement. Synthesis of allenyl ketones from propargyl alcohols
β Scribed by James M. Reuter; Robert G. Salomon
- Book ID
- 108384627
- Publisher
- Elsevier Science
- Year
- 1978
- Tongue
- French
- Weight
- 213 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0040-4039
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