Synthesis of arenes from phenols by coupling of aryl triflates with organocopper reagents
β Scribed by John E. Mc Murry; Subramaniam Mohanraj
- Book ID
- 104221357
- Publisher
- Elsevier Science
- Year
- 1983
- Tongue
- French
- Weight
- 185 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Aryl triflates react with higher order nixed cuprates R2Cu(CN)Li2 to produce arenes in good yield. The aryl ring nay have either an electron-donating or an electron-withdrawing substituknt; the organocuprate may be either primary, aryl, or vinyl.
We reported 1,2 recently a new method of regiospecific olefin synthesis diorganocuprate reagents with en01 triflates'. The reaction is general for dienol triflates, and for alkyl, aryl, and vinylic cuprates.
π SIMILAR VOLUMES
AbstractΓAryl triΒ―ates may be cross-coupled with the amino acid derived zinc reagents 1, 2 and 3 using palladium catalysis at room temperature, in the presence of anhydrous lithium chloride, conveniently yielding phenylalanine 4, b-homophenylalanine 5 and g-bishomophenylalanine 6 derivatives respect
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