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首页> 外文期刊>Australian Journal of Chemistry: A Journal for the Publication of Original Research in All Branches of Chemistry >New Macrocyclic Ligands.XVI.~* Synthesis of a Series of N-Benzylated Macrocycles Incorporating N_4O_2-Donor Sets
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New Macrocyclic Ligands.XVI.~* Synthesis of a Series of N-Benzylated Macrocycles Incorporating N_4O_2-Donor Sets

机译:新的大环配体XVI。〜*合成一系列结合N_4O_2-给体集的N-苄基化大环

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摘要

The synthesis of five 20-membered,N-benzylated macrocyclic ligands incorporating N_4O_2-donors sets and from one to three benzyl substituents for use in metal-ion recognition studies is described.The new derivatives were obtained by both benzylation of the pre-formed parent macrocycle using benzyl chloride in acetonitrile in the presence of base or,in one case,by performing macrocyclic ring closure using the appropriate N-benzylated triamine precursor by means of a bis-Schiff base condensation with the corresponding dialdehyde,followed by in situ reduction of the diamine linkages so formed.The single crystal X-ray structure of the symmetrically substituted,di-N-benzylated derivative is reported.
机译:描述了五个结合有N_4O_2-供体和一个至三个苄基取代基的20元N-苄基大环配体的合成,用于金属离子识别研究。通过预先形成的母体的两个苄基化获得新的衍生物在有碱的情况下在乙腈中使用苄基氯形成大环,或者在一种情况下,通过双Schiff碱与相应的二醛通过适当的N-苄基化三胺前体进行大环闭环,随后通过原位还原报道了对称取代的二-N-苄基化衍生物的单晶X射线结构。

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