Oxidation of 1-naphthol and related phenols with hydrogen peroxide and potassium superoxide catalysed by 5,10,15,20-tetraarylporphyrinatoiron(III)chlorides in different reaction conditions
โ Scribed by S.M.S. Chauhan; Bhanu Kalra; P.P. Mohapatra
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- English
- Weight
- 181 KB
- Volume
- 137
- Category
- Article
- ISSN
- 1381-1169
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โฆ Synopsis
Reaction of 1-naphthol and related phenols with hydrogen peroxide catalysed by 5,10,15,20-tetra pentafluorophenyl por-ลฝ . phyrinatoiron III chloride gives corresponding quinones and oxidative phenol coupled products, whereas the reaction of ลฝ . naphthols with hydrogen peroxide catalysed by 5,10,15,20-tetramesitylporphyrinatoiron III chloride give above products along with quinone epoxides in moderate yields. The reaction of quinone with potassium superoxide catalysed by ลฝ . ลฝ . Me TPPFe III Cl and p-MeOTPPFe III Cl give higher yields of quinone epoxides than the reaction of quinone with 12 ลฝ . hydrogen peroxide catalysed by 5,10,15,20-tetraarylporphyrinatoiron III chlorides.
๐ SIMILAR VOLUMES
The reaction of indole-3-acetic acid (IAA) with hydrogen peroxide catalysed by . 5,10,15,20-tetrakis(2',6'-dichloro-3'sulfonatophenyl)porphyrinatoiron(III)hydrate [Cl,TPPS,Fe(IIIWOH,),l g' tves indole-3-carbinol (IC) and indole-3-carboxaldehyde (IA) in aqueous buffer solution. The oxidation of IAA w