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首页> 外文期刊>RSC Advances >Synthesis of β-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 β-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基本磁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-酞菁 - 醇

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In this work, tetra butyl ammonium hydroxide ([Bu _(4) N]OH) and magnetic nano particles (Fe _(3) O _(4) @SiO _(2) @(CH _(2) ) _(3) NH _(2) ) were introduced as efficient catalysts for the regioselective ring opening of epoxides including aromatic and aliphatic of epoxides to give the corresponding β-phthalimido-alcohols under mild conditions. A various range of β-phthalimido-alcohols as new compounds were prepared and fully characterized by IR, ~(1) H as well as ~(13) C NMR and mass spectra. Also the synthesized compounds were studied for antioxidant properties by DPPH free radical scavenging assay. The results indicated that studied β-phthalimido-alcohols derivatives have effective antioxidant functions (IC _(50) : 0.142–0.356 mg mL ~(?1) ) in compare with BHT (IC _(50) : 0.122 mg mL ~(?1) ) and ascorbic acid (IC _(50) : 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:在这项工作中,氢氧化铵([Bu _(4)N] OH)和磁性纳米颗粒(Fe _(3)O _(4)@SiO_(2)@(CH _(2))_( 3)NH _(2))作为高效催化剂引入用于环氧化物的氧化环氧化物的区域开环,包括环氧胺的芳族和脂族,得到相应的β-邻苯胺醇在温和条件下。制备各种范围的β-酞胺 - 醇作为新化合物并用IR,〜(1)H以及〜(13)C NMR和质谱。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β-酞胺 - 醇衍生物具有有效的抗氧化功能(IC _(50):0.142-0.356mg ml〜(β1))与BHT(IC _(50):0.122mg ml〜(? 1))和抗坏血酸(IC _(50):0.146mg ml〜(β1))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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