Recently, the base-catalyeed isomarlcations ethers1 \*\* and l-to 2-olafI& bave baen reported of ally1 to propenyl to be hiShly selective in yialding the a-isomers. We wish to report on a similar isomariratioa of tert'kary ally1 ulnes which appears to be very much less selective under coadltions ess
β¦ LIBER β¦
SOLVENT EFFECTS IN THE BASE-CATALYZED ISOMERIZATION OF ALLYL TO PROPENYL ETHERS
β Scribed by Price, Charles C.; Snyder, William H.
- Book ID
- 118047342
- Publisher
- American Chemical Society
- Year
- 1961
- Tongue
- English
- Weight
- 147 KB
- Volume
- 83
- Category
- Article
- ISSN
- 0002-7863
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