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Dibenzofurans homolytic

Homolytic substitution has been little studied, and work has been confined to the reaction of dibenzofuran with carboxymethyl radicals produced from acetyl peroxide or di-tcrt-butyl peroxide in boiling acetic acid or by pyrolysis of chloroacetylpolyglycolic acids. The method of analysis of the resultant mixture of 1- (55%), 4- (30%), and 3-dibenzofuranacetic acid (15%) was crude, but the results were in accord with simple HMO calculations. The amount of the 1-substituted product is perhaps surprising in view of the steric hindrance at this position. [Pg.73]

Homolytic substitution of dibenzofuran with methoxycarbonylmethyl radicals gives poor yields of dibenzofuranacetic acids the ratio of products at the 1-, 4- and 3-positions is... [Pg.644]


See other pages where Dibenzofurans homolytic is mentioned: [Pg.550]    [Pg.500]    [Pg.925]    [Pg.550]    [Pg.331]    [Pg.319]    [Pg.35]   
See also in sourсe #XX -- [ Pg.35 , Pg.73 ]




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