Highly selective oxidative cross-coupling of substituted 2-naphthols: A convenient approach to unsymmetrical 1,1′-binaphthalene-2,2′-diols
✍ Scribed by Martin Hovorka; Jana Günterová; Jir̆í Závada
- Publisher
- Elsevier Science
- Year
- 1990
- Tongue
- French
- Weight
- 236 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0040-4039
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📜 SIMILAR VOLUMES
The oxidative coupling of 2-naphtol to 2,2Ј-dihydroxy-1,1Ј-it cannot diffuse outside the zeolite cavities through the smaller pore apertures (0.74 nm). This prediction has been binaphthyl (binaphthol) by air or oxygen has been carried out in the presence of Cu 2+ -and Fe 3+ -doped MCM-41 confirmed b
Some electron-rich 1-arylazo-2-naphthols undergo novel electrochemical oxidations, leading either to substitution by a nucleophilic aniline or to oxidative dimerisation. In the former case subsequent reduction of the azo bond provides a new route to unsymmetrical diarylamines.
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