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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

โœ 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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โœฆ 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.


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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