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• W1974489135 abstract "Treatment of the protected and unprotected nucleosides with 1,3-dibromo-5,5-dimethylhydantoin in aprotic solvents such as CH2Cl2, CH3CN, or DMF effected smooth bromination of uridine and cytidine derivatives at C-5 of pyrimidine rings as well as adenosine and guanosine derivatives at C-8 of purine rings. Addition of Lewis acids such as trimethylsilyl trifluoromethanesulfonate enhanced the efficiency of bromination." @default.
• W1974489135 created "2016-06-24" @default.
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• W1974489135 date "2012-06-01" @default.
• W1974489135 modified "2023-10-16" @default.
• W1974489135 title "Bromination at C-5 of pyrimidine and C-8 of purine nucleosides with 1,3-dibromo-5,5-dimethylhydantoin" @default.
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• W1974489135 doi "https://doi.org/10.1016/j.tetlet.2012.04.081" @default.
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