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ALLYL URAZOLE BY ALLYL IODIDE. In unpublished work on tautomerism which we completed in 1908 in our studies of cyclic amides it was shown that a large number of urazole salts and different alkyl halides undergo transformations through bi-molecular reactions. Each given urazole salt and alkyl halide gave both an 0-ester (111) and an N-ester (IV) and, with one exception, these were formed in constant ratio for different time periods. All of the facts showed that these tautomeric reactions candoi:10.1021/ja02250a014 fatcat:oihdwnzk4ra3tjzylcqysaw7cy