A solvent extraction method for separating synthetic protected oligodeoxyribonucleotides was used in our laboratory based on the lipophilic property of the protecting group of 5'-OH of the oligomers. The extraction of synthetic products protected with MMTr is complete by ether or ether-chloroform (6:1 V/V) for mononucleosides, by chloroform for dinucleoside monophosphates, by dichloromethane:n-butanol (4:1 V/V) for trimer or tetramer, and is nearly complete by dichloromethane:n-butanol (2:1 V/V) for hexamer. The 5'-end phosphorylated nucleotides, oligonucleotides and their symmetrical pyrophosphates remain in water phase. The following synthetic products of protected oligodeoxyribonucleotides have been isolated with this method, all above 85% in purity: (Formula: see text).
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Nat Commun
January 2025
Van 't Hoff Institute for Molecular Sciences, University of Amsterdam, Amsterdam, The Netherlands.
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Department of Plant Sciences, North Dakota State University.
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State Key Laboratory of Organic-Inorganic Composites, College of Life Science and Technology, Beijing University of Chemical Technology, No. 15 East Road of North Third Ring Road, Chao Yang District, Beijing 100029, China. Electronic address:
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Faculty of Pharmacy and Medical Sciences, University of Petra, Amman, 11196, Jordan.
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View Article and Find Full Text PDFTrop Biomed
December 2024
Department of Entomology and Plant Pathology, Khon Kaen University, Thailand Mittapap Road, Khon Kaen, Khon Kaen, 40002, Thailand.
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