Electron-rich biphenyls were selectively oxyfunctionalised through a halogenation-methoxylation sequence. The obtained biphenyl methyl ethers were then oxidised to the corresponding quinones. This strategy transforms commercially available biphenyls into both natural and bioactive oxidised compounds.
Regioselective halogenation of biphenyls for preparation of valuable polyhydroxylated biphenyls and diquinones
Paolo Bovicelli;Roberto Antonioletti;Davide Fabbri;Maria Antonietta Dettori
2006
Abstract
Electron-rich biphenyls were selectively oxyfunctionalised through a halogenation-methoxylation sequence. The obtained biphenyl methyl ethers were then oxidised to the corresponding quinones. This strategy transforms commercially available biphenyls into both natural and bioactive oxidised compounds.File in questo prodotto:
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