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Arylation of 6H-dibenzo[c,e][1,2ℷ5]oxaphosphinine 6-oxide

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RUSSIAN JOURNAL OF ORGANIC CHEMISTRY
卷 40, 期 12, 页码 1782-1786

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MAIK NAUKA/INTERPERIODICA
DOI: 10.1007/s11178-005-0099-9

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Arylation and alkylation of 6H-dibenzo[c,e][1,2lambda(5)]oxaphosphinine 6-oxide at the phosphorus atom was accomplished. Tetrafluoro-4-pyridyl fragment was introduced via reaction of 6-trimethylsiloxy-6H-dibenzo[c,e][1,2]oxaphosphinine with pentafluoropyridine. The arylation of the title compound with aryl iodides containing both electron-acceptor and electron-donor substituents was effected under catalysis by palladium or nickel complexes.

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