Hydrolysis of the flavin (5) with Triton B gave the 4a-spirohydantoin (6) as the major product together with, among other products, the imidazo[4,5-b]quinoxaline (7). Formation of such products indicates that nucleophilic attack by hydroxide ion on the flavin ring had occurred preferentially at the 10a-position.
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HARAYAMA et al. (1987) studied this question.
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