Please use this identifier to cite or link to this item: https://zone.biblio.laurentian.ca/handle/10219/2699
Title: The synthesis of macrocyclic molecules related to telomestatin
Authors: Aldarini, Wafa Saeed S.
Keywords: G-quadruplexes;telomestatin;poly-oxazole macrocycles;macrocyclization;dinuclear copper (II) complex
Issue Date: 13-Jan-2017
Abstract: G-quadruplex DNA represents an attractive target for the development of anti-cancer therapeutic agents as it plays important roles in transcriptional regulation and the maintenance of telomeric length. Oxazole-containing macrocycles such as telomestatin are considered to be a promissing new class of G-quadruplex binding ligands. In this work, poly-oxazole building blocks were synthesized to prepare a tetraoxazole peptide macrocycle in good yield. The macrocycle was obtained by employing standard peptide coupling conditions using a convergent solution phase approach. The synthetic unit of the oxazole amino acid containing compound was prepared by cyclodehydration/oxidation of protected serine and phenylalanine. Two-cycle coupling of the unit gave a linear tetraoxazole amide. The final macrocyclization was accomplished by using O-[(1-cyano-2-ethoxy-2-oxoethylidene)amino]-oxytri(pyrrolidin-1-yl) phosphonium hexafluorophosphate (PyOxP) and the product (45% yield) was characterized by 1H NMR. Finally, the Cu (II) coordination chemistry of the tetraoxazole macrocycle was investigated by spectrophotometric titration.
URI: https://zone.biblio.laurentian.ca/handle/10219/2699
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Master's Theses

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