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首页> 外文期刊>Synthesis: International Journal of Methods in Synthetic Organic Chemistry >Synthesis of N-Aryl and N-Heteroaryl gamma-, delta-, and epsilon-Lactams Using Deprotometalation-Iodination and N-Arylation, and Properties Thereof
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Synthesis of N-Aryl and N-Heteroaryl gamma-, delta-, and epsilon-Lactams Using Deprotometalation-Iodination and N-Arylation, and Properties Thereof

机译:使用去脱蛋白 - 碘化和N-芳基化合成N-芳基和N-杂芳基γ-,δ和ε-内酰胺,及其性质

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摘要

Xanthone, thioxanthone, fluorenone, benzophenone, 2-benzoylpyridine, dibenzofuran, and dibenzothiophene were deprotonated using a base prepared in situ from MCl2TMEDA (M = Zn or Cd; TMEDA =N,N,N,N-tetramethylethylenediamine) and lithium 2,2,6,6-tetramethylpiperidide in a 1:3 ratio, as demonstrated by subsequent iodolysis. The different aryl halides were involved as partners in the N-arylation of pyrrolidin-2-one. In the presence of copper(I) iodide and tripotassium phosphate, and using dimethyl sulfoxide as solvent, the reactions could be performed in yields ranging from 40 to 70%. Most of the products were tested for their antimicrobial, antifungal, antioxidant, and cytotoxic (MCF-7) activity.
机译:使用原位制备的碱从MCL2 <粗体> TMEDA (M = Zn或CD; TMEDA = N,N,N,N,N,N,N,N,N,N,N,N,N,N,N,N,N,N,N,N,N,N,N,N,N,N,N,N,N - 通过随后的碘解证明,1-Tamethylendi金属和锂2,2,6,6-四甲基哌啶鎓为1:3的比例。 将不同的芳基卤化物作为吡咯烷-2-一体的N-芳基化的合作伙伴涉及。 在铜(I)碘化铜和磷酸辛酸磷酸辛酸碘化磷酸盐存在下,并使用二甲基亚砜作为溶剂,可以以40-70%的产率进行反应。 大多数产品用于其抗微生物,抗真菌,抗氧化剂和细胞毒性(MCF-7)活性测试。

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