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首页> 外文期刊>RSC Advances >Synthesis of beta-phthalimido-alcohols via regioselective ring opening of epoxide by using reusable basic magnetic nano particles and their biological investigation
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Synthesis of beta-phthalimido-alcohols via regioselective ring opening of epoxide by using reusable basic magnetic nano particles and their biological investigation

机译:通过使用可重复使用的碱性纳米颗粒及其生物调查,通过环氧化物的区域选择性环的合成β-酞胺 - 醇

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In this work, tetra butyl ammonium hydroxide ([Bu4N]OH) and magnetic nano particles (Fe3O4@SiO2@(CH2)(3)NH2) were introduced as efficient catalysts for the regioselective ring opening of epoxides including aromatic and aliphatic of epoxides to give the corresponding beta-phthalimido-alcohols under mild conditions. A various range of beta-phthalimido-alcohols as new compounds were prepared and fully characterized by IR, H-1 as well as C-13 NMR and mass spectra. Also the synthesized compounds were studied for antioxidant properties by DPPH free radical scavenging assay. The results indicated that studied beta-phthalimido-alcohols derivatives have effective antioxidant functions (IC50: 0.142-0.356 mg mL(-1)) in compare with BHT (IC50: 0.122 mg mL(-1)) and ascorbic acid (IC50: 0.146 mg mL(-1)) as standards. This may be a new health-care food and drug supplement for special use in the future.
机译:在该作品中,将氢氧化铵([Bu4N] OH)和磁性纳米颗粒(Fe 3 O 4 OH)(Fe 3 O 4)(Fe 3 O 4)(3)NH2)作为有效催化剂,包括环氧化物的区域选择性环开口,包括环氧胺的芳族和脂族 在温和条件下给予相应的β-酞米胺 - 醇。 制备各种范围的β-酞米胺 - 作为新化合物的醇,并用IR,H-1以及C-13 NMR和质谱进行了完全表征。 通过DPPH自由基清除测定,研究了合成化合物的抗氧化性能。 结果表明,研究的β-酞胺 - 醇衍生物具有有效的抗氧化功能(IC50:0.142-0.356mg ml(-1)),与BHT(IC 50:0.122mg ml(-1))和抗坏血酸(IC50:0.146 Mg ml(-1))作为标准。 这可能是未来特殊用途的新保健食品和药物补充剂。

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