ChemInform Abstract: Sterically Hindered 1,3-Diketones in the Michael Reaction.
β Scribed by I. E. SOKOLOV; A. S. ZANINA; S. I. SHERGINA; M. S. SHVARTSBERG
- Book ID
- 112033628
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 29 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0931-7597
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π SIMILAR VOLUMES
Acylation of Sterically Hindered 2-Propargyl-1,3-diketones. -The acylation of sterically hindered propargyl-substituted 1,3-diketones (I) by acyl chlorides occurs selectively at the terminal acetylenic group in the presence of CuCl. Some peculiarities of this reaction are reported. -(SHERGINA, S. I.
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Ring-Chain Tautomerism, Oxidation, and NO-Reaction of a Sterically Hindered 1,3-Dihydroxyimidazolidine. -The title compounds (III) and (IV) are prepared as spin-traps for the detection of NO. -(WEBER,