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- W2053502743 abstract "Abstract The synthesis of a series of 2,3‐diarylbenzo[ b ]furans starting from 1,2‐diarylethanones and 1,2‐dibromoarenes proceeds by means of both homogeneous and polymer‐anchored palladium catalysts. This tandem process can be effectively halted at the C ‐arylation step, thus providing key o ‐bromoarylated deoxybenzoin intermediates in good yields. The efficient oxidative coupling leading to benzo[ b ]phenanthro[9,10‐ d ]furans is carried out using the safer hypervalent iodine reagent PIFA. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005)" @default.
- W2053502743 created "2016-06-24" @default.
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- W2053502743 date "2005-06-01" @default.
- W2053502743 modified "2023-10-16" @default.
- W2053502743 title "A New, Expeditious Entry to the Benzophenanthrofuran Framework by a Pd‐Catalyzed <i>C</i>‐ and <i>O</i>‐Arylation/PIFA‐Mediated Oxidative Coupling Sequence" @default.
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- W2053502743 doi "https://doi.org/10.1002/ejoc.200400856" @default.
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