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ChemInform Abstract: General Synthesis of α-Acetoxy Ethers from Esters by DIBALH Reduction and Acetylation.
✍ Scribed by V. H. DAHANUKAR; S. D. RYCHNOVSKY
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 34 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0931-7597
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✦ Synopsis
General Synthesis of α-Acetoxy Ethers from Esters by DIBALH Reduction and Acetylation.
-The mechanism for the formation of title products, e.g. (III), (V), and (VII), is discussed. The α-acetoxy esters are versatile 1,3-diol synthons that can serve as starting material for the synthesis of further products via carbon-carbon bond formation. -(DAHANUKAR,
📜 SIMILAR VOLUMES
Synthesis of Esters from Silyl Ethers and Acyl Chlorides: Catalysis by Quaternary Ammonium Chlorides. -Quaternary ammonium chlorides are more efficient than other ammonium halides as catalysts in the title reaction. Acetyl chloride reacts faster than benzoyl chloride and trimethylsilyl ethers react