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首页> 外文期刊>Polyhedron: The International Journal for Inorganic and Organometallic Chemistry >Synthesis of oxonium derivatives of the dodecahydro-closo-dodecaborate anion [B12H12](2-). Tetramethylene oxonium derivative of [B12H12](2-) as a convenient precursor for the synthesis of functional compounds for boron neutron capture therapy
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Synthesis of oxonium derivatives of the dodecahydro-closo-dodecaborate anion [B12H12](2-). Tetramethylene oxonium derivative of [B12H12](2-) as a convenient precursor for the synthesis of functional compounds for boron neutron capture therapy

机译:十二氢-氯-十二-癸酸酯阴离子[B12H12](2-)的氧鎓衍生物的合成。 [B12H12](2-)的四亚甲基氧鎓衍生物作为方便的前体,用于合成硼中子俘获疗法的功能化合物

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摘要

Direct synthesis of oxonium derivatives of the dodecahydro-closo-dodecaborate anion is described and the reaction mechanism is discussed. Various derivatives of the [B12H12](2-) anion containing hydroxyl, amine, acid, and amino acid functions were prepared by ring opening reactions of the tetramethylene oxonium derivative [B12H11O(CH2)(4)](-) with different nucleophiles. This approach is suitable for the development of compounds to be used in tumour selective boron neutron capture therapy (BNCT) and as linkers for the attachment of radioactive halogen labels for radioimmunodetection and radioimmunotherapy. (C) 2000 Elsevier Science Ltd All rights reserved. [References: 34]
机译:描述了十二氢-氯-十二-癸酸酯阴离子的氧鎓衍生物的直接合成,并讨论了其反应机理。通过四亚甲基氧鎓衍生物[B12H11O(CH2)(4)](-)与不同亲核试剂的开环反应,制备了具有羟基,胺基,酸基和氨基酸官能团的[B12H12](2-)阴离子的各种衍生物。该方法适合于开发用于肿瘤选择性硼中子捕获疗法(BNCT)的化合物,并用作连接放射性卤素标记物以进行放射免疫检测和放射免疫疗法的接头。 (C)2000 Elsevier Science Ltd保留所有权利。 [参考:34]

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