A mild and efficient protocol for the ipso-hydroxylation of arylboronic acids
- 1 February 2013
- journal article
- research article
- Published by Elsevier BV in Tetrahedron Letters
- Vol. 54 (14), 1821-1823
- https://doi.org/10.1016/j.tetlet.2013.01.079
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- Copper-catalyzed direct preparation of phenols from aryl halidesCatalysis Communications, 2010
- Palladium‐Catalyzed Hydroxylation of Aryl Halides under Ambient ConditionsAngewandte Chemie-International Edition, 2009
- Practical Imidazole‐Based Phosphine Ligands for Selective Palladium‐Catalyzed Hydroxylation of Aryl HalidesAngewandte Chemie-International Edition, 2009
- Palladium Nanoparticles Supported on Polyaniline Nanofibers as a Semi‐Heterogeneous Catalyst in WaterAngewandte Chemie-International Edition, 2007
- Palladium‐Catalyzed Coupling of Ammonia and Hydroxide with Aryl Halides: The Direct Synthesis of Primary Anilines and PhenolsAngewandte Chemie-International Edition, 2007
- Palladium-catalyzed C–O bond formation: direct synthesis of phenols and aryl/alkyl ethers from activated aryl halidesTetrahedron Letters, 2007
- The Selective Reaction of Aryl Halides with KOH: Synthesis of Phenols, Aromatic Ethers, and BenzofuransJournal of the American Chemical Society, 2006
- Sandmeyer reactions. Part 7.1 An investigation into the reduction steps of Sandmeyer hydroxylation and chlorination reactionsJournal of the Chemical Society, Perkin Transactions 2, 2002
- Alcohols, ethers and phenolsJournal of the Chemical Society, Perkin Transactions 1, 2000
- Boronic Esters in Stereodirected SynthesisTetrahedron, 1989