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Convenient Cleavage Reaction of 1-Acylhydantoin to Amide

Convenient Cleavage Reaction of 1-Acylhydantoin to Amide
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摘要 A cleavage reaction of 1-acylhydantoin by an amine in tetrahydrofuran at elevated temperature provided the corre-sponding amide and hydantoin in high yield. It was found that the addition of diethylaluminum chloride accelerated the cleavage reaction rate. The amide yield depended on the steric hindrance of the amine. A cleavage reaction of 1-acylhydantoin by an amine in tetrahydrofuran at elevated temperature provided the corre-sponding amide and hydantoin in high yield. It was found that the addition of diethylaluminum chloride accelerated the cleavage reaction rate. The amide yield depended on the steric hindrance of the amine.
出处 《International Journal of Organic Chemistry》 2013年第3期194-197,共4页 有机化学国际期刊(英文)
关键词 AMIDES Acylhydantoin Chiral AUXILIARIES CLEAVAGE LEWIS Acid Amides Acylhydantoin Chiral Auxiliaries Cleavage Lewis Acid
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