Oxidative Coupling of 2-Naphthols Catalysed by Cu-Exchanged Montmorillonite
- 1 August 1996
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 26 (16) , 3075-3079
- https://doi.org/10.1080/00397919608004610
Abstract
Cu-exchanged montmorillonite catalyses the oxidative coupling of 2-naphthols under aerated conditions.Keywords
This publication has 15 references indexed in Scilit:
- Catalytic asymmetric oxidation of sulfides to sulfoxides with tert-butyl hydroperoxide using binaphthol as a chiral auxiliaryThe Journal of Organic Chemistry, 1993
- Expedient route to 3- and 3,3′-substituted 1,1′-bi-2-naphthols by directed ortho metalation and suzuki cross coupling methodsTetrahedron Letters, 1992
- Synthesis and Applications of Binaphthylic C2-Symmetry Derivatives as Chiral Auxiliaries in Enantioselective ReactionsSynthesis, 1992
- Oxidative coupling reactions of phenols with iron(III) chloride in the solid stateThe Journal of Organic Chemistry, 1989
- Centenary Lecture. Chemical multiplication of chirality: science and applicationsChemical Society Reviews, 1989
- Synthesis and chiral recognition of optically active crown ethers incorporating a biphenanthryl moiety as the chiral centreJournal of the Chemical Society, Chemical Communications, 1984
- Asymmetric phenol oxidation. Stereospecific and stereoselective oxidative coupling of a chiral tetrahydronaphtholThe Journal of Organic Chemistry, 1981
- Biomimetic asymmetric oxidative coupling of phenolsBioorganic Chemistry, 1978
- Oxidative phenol coupling with cupric-amine complexesTetrahedron Letters, 1977
- Oxidative coupling of phenolsJournal of the American Chemical Society, 1968