Ein neuer Zugang zu 2′-O-(2-Methoxyethyl)ribonucleosiden ausgehend vonD-Glucose
Author:
Publisher
Wiley
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis
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1. TricycloDNA-modified oligo-2′-deoxyribonucleotides reduce scavenger receptor B1 mRNA in hepatic and extra-hepatic tissues—a comparative study of oligonucleotide length, design and chemistry;Nucleic Acids Research;2012-03-30
2. Synthesis and hybridization of 2′-O-methyl-RNAs incorporating 2′-O-carbamoyluridine and unique participation of the carbamoyl group in U–G base pair;Bioorganic & Medicinal Chemistry;2009-10
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4. Process Research on the Preparation of DMT Protected 2′-O-Methoxyethylguanosine for Oligonucleotide Synthesis in Therapeutic Applications;Nucleosides, Nucleotides and Nucleic Acids;2008-08-18
5. A General Method for the Synthesis of 2‘-O-Cyanoethylated Oligoribonucleotides Having Promising Hybridization Affinity for DNA and RNA and Enhanced Nuclease Resistance;The Journal of Organic Chemistry;2005-11-10
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