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Design and synthesis of Pyrimidine C-Nucleosides, 5-Polyfluoroalkyl-5-deazaalloxazines and Spiro[pyrimido[4,5-b]quinoline-3',5-indoline-2'-one]-3,10-dihydro-2,4-diones  (  Dissertationsschrift  ) 
A wide range of novel 2-(b-D-ribofuranosyl)pyrimidines was synthesized by 3+3 cyclocondensation. Reaction of 6-arylamino-1,3-dialkyluracils with perfluorinated carboxylic acid anhydrides or chloroanhydrides and subsequent cyclization gave the corresponding 1,3-dialkyl-5-(polyfluoroalkyl)-5-deazaalloxazines. An unexpected recyclization in the series of spiro[indole-3,5'-pyrimido[4,5-b]quinoline]-2,2',4'-trione derivatives, carried out via a reaction between (thio)barbituric acids, isatins and electron-rich aromatic amines, was observed.
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