首页> 外国专利> Method of synthesis of new compounds disaccharide, without the glycoside junction, the products obtained by this process and their applications as surfactant, or chelating agent.

Method of synthesis of new compounds disaccharide, without the glycoside junction, the products obtained by this process and their applications as surfactant, or chelating agent.

机译:没有糖苷键的新化合物二糖的合成方法,通过该方法获得的产物及其作为表面活性剂或螯合剂的应用。

摘要

We have prepared new disaccharide compounds associating, without any glycoside link, two derivatives of oses or of itols A and B, on sites chosen in advance of formula I: IMAGE The process for the synthesis of these compounds includes especially the stage of linking the units A and B by attack of a derivative of the unit B, in alcoholate form, on an anhydro group derived from the unit A. The products obtained bear, respectively, 0 to 3 ZIFI groups on the unit A and 0 to 3 ZJGJ groups on the unit B, as well as a modulable number of free OH groups which can vary from 0 to 4 (p) on the unit A and from 0 to 4 (p') on the unit B. The units A and B may create a second link by internal cyclisation. One of the groups ZIFI or ZJGJ may be a third unit C analogous to A and B, resulting in trisaccharide compounds. In addition, if the unit C is joined to B, it may also create a link with A by internal cyclisation and if the unit C is joined to A, it may also create a link with B by internal cyclisation. The surface-active, chelating and biological properties revealed by the products obtained are described with a view to applications as surface and/or chelating agents, calcium antagonist medications and antitumour medications.
机译:我们已经制备了新的二糖化合物,其在糖苷连接下没有任何糖苷连接,在式I预先选择的位点上将糖或糖醇A和糖醇B的两个衍生物缔合:这些化合物的合成过程尤其包括连接阶段通过醇形式的单元B的衍生物对衍生自单元A的脱水基团的攻击而攻击单元A和B。获得的产物分别在单元A上具有0至3个ZIFI基团和0至3个ZJGJ单元B上的基团,以及可调节数量的游离OH基团,其在单元A上可从0变为4(p),在单元B上可从0变为4(p')。单元A和B可以通过内部循环化创建第二个链接。 ZIFI或ZJGJ基团之一可以是类似于A和B的第三单元C,产生三糖化合物。此外,如果单元C连接到B,则它还可以通过内部环化与A建立链接,如果单元C连接到A,则它也可以通过内部环化与B建立链接。描述了所获得的产品所揭示的表面活性,螯合和生物学性质,以作为表面和/或螯合剂,钙拮抗剂药物和抗肿瘤药物的应用来描述。

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