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Electro-oxidative N-Halogcnation of 2-Azetidinone Derivatives.Reaction of N-Halo-2-azetidinones

机译:2-氮杂萘酮衍生物的电氧化N-卤素。N-卤代2-氮杂萘酮的反应

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Penems and carbapenems have attracted keen interest as promising antibiotics owing to their potent and broad antimicrobial activities as well as excellent metabolic stability.4-Acetoxy-2-azetidinone 1 and N-halo-2-azetidinones 2 have been reported as a key intermediates for synthesis of the important class of beta-lactam antibiotics.We investigated electrolysis of 2-azetidinone 3 affording 1,2a and 2b depending on the choice of the electrolysis media and/or procedure (Scheme 1).
机译:Penems和Carbapenems由于它们的有效性和广泛的抗微生物活性以及优异的代谢稳定性而吸引了耐受性的抗生素.4-乙酰氧基-2-氮化萘醌1和N-Halo-2-氮化萘醌2作为一个关键的中间体重要种类的β-内酰胺抗生素等类别。根据电解介质和/或程序的选择,所研究的2-氮杂萘酮3的电解,得到1,2a和2b(方案1)。

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