Department of Chemistry, Université de Montréal , Montréal, QC, H3C 3J7, Canada.
J Org Chem. 2013 Sep 20;78(18):9064-75. doi: 10.1021/jo401170y. Epub 2013 Sep 4.
A constrained tricyclic analogue of α-L-LNA (2), which contains dual modes of conformational restriction about the ribose sugar moiety, has been synthesized and characterized by X-ray crystallography. Thermal denaturation experiments of oligonucleotide sequences containing this tricyclic α-L-LNA analogue (α-L-TriNA 2, 5) indicate that this modification is moderately stabilizing when paired with complementary DNA and RNA, but less stabilizing than both α-L-LNA (2) and α-L-TriNA 1 (4).
已合成并通过 X 射线晶体学对含有核糖部分双模式构象限制的α-L-LNA(2)三环类似物进行了表征。含有该三环α-L-LNA 类似物(α-L-TriNA 2,5)的寡核苷酸序列的热变性实验表明,与互补 DNA 和 RNA 配对时,这种修饰具有中等程度的稳定性,但不如α-L-LNA(2)和α-L-TriNA 1(4)稳定。