Bromination of Pyrimidines by N-Bromosuccinimide. III. Bromination of Anilino-and Phenoxypyrimidines.
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概要
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2-Aminopyrimidines were brominated at their C_5-positions predominantly with NBS in carbon tetrachloride in spite of the presence of an anilino-, haloanilino-, or phenoxygroup at their c_6-positions as substituents.
- 公益社団法人日本薬学会の論文
- 1962-11-25
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関連論文
- Synthesis of 2,4,6-Triphenyloxazolo-[5,4-d] pyrimidine-5-thione-7-one
- Bromination of Pyrimidines by N-Bromosuccinimide. III. Bromination of Anilino-and Phenoxypyrimidines.