Palladium-Catalyzed 1,4-Acetoxy-trifluoroacetoxylation and 1,4-Alkoxy-trifluoroacetoxylation of Cyclic 1,3-Dienes. Scope and Mechanism. -The title products are yielded with good regio-and stereoselectivities. The stereochemical outcome of the acetoxylation of cyclohexadiene (I) can be reversed by
✦ LIBER ✦
Palladium-catalyzed 1,4-acetoxy-trifluoroacetoxylation of 1,3-dienes
✍ Scribed by Jan-E. Bäckvall; Jan V»gberg; Ruth E. Nordberg
- Publisher
- Elsevier Science
- Year
- 1984
- Tongue
- French
- Weight
- 278 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
Palladium-catalyzed oxidation of conjugated dienes in acetic acid containing CF3COOH/Li00CCF3 results in the formation of I-acetoxy-4-trifluoroacetoxy-2-alkenes.
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