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The chemotherapy of asymmetric ligand neutron therapy disease and tumour

机译:不对称配体中子的化学疗法治疗疾病和肿瘤

摘要

The present invention is to be related to the whereA asymmetric ligands of general formula I, M is hydrogen or tert-butyl, and D is hydrogen-CH2-Ar, and Ar is the aryl with 6 carbon atoms, there can be 1-9 carbon atom with alkyl one or disubstituted, or structure OCH2 (CH2OCH2) nCH2-O-Z, wheren of 2-thienyl, X are numbers 0,1,2, Z is hydrogen, alkyl C1arrives C6, benzyl or B groups (OH) 2, and wherein B is atomic boron. The racemic or chipal compounds of asymmetric ligand. To be based on known facts be alcohol benzyl keys in acid medium the is easy ionization of its method prepared is reacted with the cationic nucleophilic reagent of above-mentioned origin. In the case where us, from the alcohol (two) being easily accessible in Formula II, M has above-mentioned definition, and T is hydrogen or group-CH2OH. The general formula II reactions of derivative be easy to aromatics and miscellaneous material rich in electronics and in acid condition, they provide the product of general formula IIIs, and here, M, D, Ar are with above-mentioned meaning. These compounds are interesting ligands, furthermore, it is possible to be converted into seeking I. by well known methodThe compound ofIMAGEgeneral formula
机译:本发明涉及其中通式I的不对称配体,M为氢或叔丁基,D为氢-CH 2 -Ar,且Ar为具有6个碳原子的芳基,可以有1-9个。具有一个或两个取代的烷基的碳原子,或结构为OCH2(CH2OCH2)nCH2-OZ,其中2-噻吩基中的n,X为0,1,2,Z为氢,烷基C 1取代C 6,苄基或B基团(OH)2,其中B是原子硼。不对称配体的外消旋或碎片化合物。基于已知的事实是在酸性介质中的醇苄基键,其制备的方法易于电离,使其与上述来源的阳离子亲核试剂反应。在我们的情况下,在式II中易于获得的醇(两种)中,M具有上述定义,并且T是氢或-CH 2 OH基团。衍生物的通式II的反应易于在芳族化合物和富含电子且在酸性条件下的杂物中进行,它们提供了通式III的产物,在此,M,D,Ar具有上述含义。这些化合物是令人感兴趣的配体,此外,可以通过众所周知的方法转化为寻找I。通式的化合物

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