Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, Russian Journal of Organic Chemistry called The First Analog of Pyrimidine Nucleosides with Two Nucleobases and Two D-Ribofuranose Residues, Author is Andreeva, O. V.; Saifina, L. F.; Belenok, M. G.; Semenov, V. E.; Kataev, V. E., which mentions a compound: 111-24-0, SMILESS is BrCCCCCBr, Molecular C5H10Br2, SDS of cas: 111-24-0.
The reaction of 1,5-bis[1-(prop-2-yn-1-yl)uracil-3-yl]pentane with 2′,3′,5′-tri-O-acetyl-β-D-ribofuranosylazide followed by removing of acetyl protective groups with a solution of sodium methylate in methanol afforded 1,5-bis{[1-methyl(β-D-ribofuranosyl)-1H-1,2,3-triazole-4-yl]uracil-3-yl}pentane which is the first analog of pyrimidine nucleosides with two nucleobases and two D-ribofuranose residues.
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Reference:
Chiral nitrogen ligands in late transition metal-catalysed asymmetric synthesis—I. Addressing the problem of ligand lability in rhodium-catalysed hydrosilations,
Nitrogen-Containing Ligands for Asymmetric Homogeneous and Heterogeneous Catalysis