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首页> 外文期刊>Bulletin of the Korean Chemical Society >A Novel Synthesis of N-Methoxy-N-methylamides from 4,6-Pyrimidyl Urethane and Grignard Reagents
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A Novel Synthesis of N-Methoxy-N-methylamides from 4,6-Pyrimidyl Urethane and Grignard Reagents

机译:由4,6-嘧啶氨基甲酸酯和格氏试剂新颖合成N-甲氧基-N-甲基酰胺

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摘要

The N-methoxy-N-methylamides (Weinreb amides) have enjoyed tremendous popularity because they react with organometallics (RM,M=Li,MgX) to provide various ketones through stable metal-chelated intermediates without side products.1 Among the various methods for the preparation of N-memoxy-N-methylamides,the condensation of carboxylic acids and N,O-dimethylhydroxylamine hydrochloride (MeONH2MeCl) using peptide coupling reagents has been frequently employed.
机译:N-甲氧基-N-甲基酰胺(Weinreb酰胺)之所以广受青睐,是因为它们与有机金属(RM,M = Li,MgX)反应,通过稳定的金属螯合的中间体生成副酮,而没有副产物。1 N-甲氧基-N-甲基酰胺的制备,羧酸与N,O-二甲基羟胺盐酸盐(MeONH2MeCl)的缩合反应经常使用肽偶联剂。

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