Reaction of peroxy-p-quinol acetates with trifluoroacetic anhydride. Formation of new oxepinone derivatives.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference9 articles.
1. A NOVEL BASE-CATALYZED REARRANGEMENT OFp-PEROXYQUINOL ESTERS
2. Base-catalyzed decomposition of 3,5-di--butyl-4-hydroxybenzoic esters of -peroxyquinols derived from 2,6-di--Butylphenols
3. Acylation of 4-substituted 6-hydroperoxy-2,6-di--butyl-2,4-cyclohexadienones
4. Acid-catalyzed reaction of 2,6-di--butyl-4-hydroperoxy-2,5-cyclohexadienones and their acetates
5. Peroxy esters—III
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Evidence for the Mechanism of Hydroxylation by 4-Hydroxyphenylpyruvate Dioxygenase and Hydroxymandelate Synthase from Intermediate Partitioning in Active Site Variants;Biochemistry;2011-08-16
2. Novel Reduction of 2,6-Di-t-butyl-p-quinols with Sodium Borohydride;Chemistry Letters;1994-05
3. ChemInform Abstract: PEROXY ESTERS. V. REACTION OF PEROXY-P-QUINOL ACETATES WITH TRIFLUOROACETIC ANHYDRIDE. FORMATION OF NEW OXEPINONE DERIVATIVES;Chemischer Informationsdienst;1980-07-29
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