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ChemInform Abstract: Regioselective Conversion of Arylboronic Acids to Phenols and Subsequent Coupling to Symmetrical Diaryl Ethers.

✍ Scribed by Juergen Simon; Stefan Salzbrunn; G. K. Surya Prakash; Nicos A. Petasis; George A. Olah

Book ID: 101912133
Publisher: John Wiley and Sons
Year: 2010
Weight: 28 KB
Volume: 32
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200124087

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📜 SIMILAR VOLUMES

Regioselective Conversion of Arylboronic

Regioselective Conversion of Arylboronic Acids to Phenols and Subsequent Coupling to Symmetrical Diaryl Ethers

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ChemInform Abstract: Synthesis of Diaryl

ChemInform Abstract: Synthesis of Diaryl Ethers Through the Copper-Promoted Arylation of Phenols with Arylboronic Acids. An Expedient Synthesis of Thyroxine.

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ChemInform Abstract: [Pd(L)Cl2]-Catalyze

ChemInform Abstract: [Pd(L)Cl2]-Catalyzed Selective Hydroxylation of Arylboronic Acids to Phenols.

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ChemInform Abstract: An Optimized Pallad

ChemInform Abstract: An Optimized Palladium Catalyzed Cross-Coupling of Nonracemic Trifluoromethylsulfonyl and Fluorosulfonyl Enol Ethers to Arylboronic Acids.

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ChemInform Abstract: Palladium/Phosphite

ChemInform Abstract: Palladium/Phosphite or Phosphate Catalyzed Oxidative Coupling of Arylboronic Acids with Alkynes to Produce 1,4-Diaryl-1,3-butadienes.

✍ Hakaru Horiguchi; Hayato Tsurugi; Tetsuya Satoh; Masahiro Miura 📂 Article 📅 2008 🏛 John Wiley and Sons ⚖ 42 KB

ChemInform Abstract: Micellar System in

ChemInform Abstract: Micellar System in Copper-Catalyzed Hydroxylation of Arylboronic Acids: Facile Access to Phenols.

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## Abstract An efficient method for the Cu‐catalyzed oxidative hydroxylation of arylboronic acids under mild, ligand‐ and base‐free conditions in water containing an amphiphilic surfactant is described.