Electron-rich biphenyls were selectively oxyfunctionalised throw a halogenation-methoxylation sequence. The obtained biphenyl methyl ethers were then oxidized to the corresponding quinines. This strategy transforms commercially available biphenyls to both natural and bioactive oxidized 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 throw a halogenation-methoxylation sequence. The obtained biphenyl methyl ethers were then oxidized to the corresponding quinines. This strategy transforms commercially available biphenyls to both natural and bioactive oxidized compounds.File in questo prodotto:
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