首页> 外文期刊>Indian Journal of Chemistry, Section B. Organic Including Medicinal >Thienopyrimidines as hetryl moiety in 2-azetidinones:Synthesis of 4-hetryl-2-azetidinones
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Thienopyrimidines as hetryl moiety in 2-azetidinones:Synthesis of 4-hetryl-2-azetidinones

机译:噻吩并嘧啶类作为2-氮杂环丁酮中的hetryl部分:4-hetryl-2-azetidinones的合成

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摘要

A Facile and efficient method for the synthesis of 4-hetryl substituted beta-lactams 1 have been reported from substituted thienopyrimidinone 2b,which in turn was prepared from appropriately substituted 2-amino-3-carboxamido thiophene 10.The structures of newly synthesized compounds have been established through spectral and analytical analysis.It is evident from the literature that both thienopyrimidinone and 2-azetidinones are well known for their varied biological activities such as high affinity selective 5-HT_(1A)receptor ligands,potential anti-hypertensive agents,molluscicidal and larvicidal activities,anticonvulsant and anti-bacterial activity,and cholesterol inhibition activity.
机译:已经报道了由取代的噻吩并嘧啶酮2b合成4-己烯基取代的β-内酰胺1的简便有效方法,而噻吩并嘧啶酮2b则由适当取代的2-氨基-3-羧酰胺基噻吩10制备。新合成的化合物的结构具有通过光谱和分析分析确定了噻吩并嘧啶酮和2-氮杂环丁酮的生物活性,如高亲和力的选择性5-HT_(1A)受体配体,潜在的降压药,杀软体动物作用,这是众所周知的。和杀幼虫活性,抗惊厥和抗菌活性以及胆固醇抑制活性。

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