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The benzoylation of uracil and thymine
Authors:Kenneth A Cruickshank  Josef Jiricny  Colin B Reese
Institution:Department of Chemistry, King''s College, Strand, London WC2R 2LS, England
Abstract:Uracil and thymine react with benzoyl chloride in acetonitrile-pyridine solution at room temperature to give first their 1-N-benzoyl (2b and 3b) and then their 1-N, 3-N-dibenzoyl derivatives (4a and 4b, respectively); the latter compounds are converted into the corresponding 3-N-benzoyl derivatives (5a and 6a) under mild conditions of basic hydrolysis.
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