Synthesis of pentathymidylate using a 4-monomethoxytritylthio (MMTrS) group as a 5′-hydroxyl protecting group: toward oligonucleotide synthesis without acid treatment
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference12 articles.
1. The chemistry of sulfenamides
2. The TDE sulfenyl group as a protective group for amines
3. A New Method for the Preparation of 3-Nitro-2-pyridinesulfenyl Chloride and One-Pot Syntheses ofN(α)-tert-butoxycarbonyl-S-3-nitro-2-pyridinesulfenyl Derivatives of Cysteine and D-Penicillamine
4. Triphenylmethanesulfenyl Group. A New Protecting Group for the Uracil Residue in Oligoribonucleotide Synthesis
Cited by 12 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Synthesis of Branched DNA Using Oxidatively Cleavable Tritylsulfenyl as a Hydroxy Protecting Group;Current Protocols in Nucleic Acid Chemistry;2014-09
2. Protection for the Hydroxyl Group, Including 1,2- and 1,3-Diols;Greene's Protective Groups in Organic Synthesis;2014-08-11
3. A facile and highly stereoselective synthesis of 1-thiotrehalose;Tetrahedron Letters;2012-08
4. ChemInform Abstract: Synthesis of Pentathymidylate Using a 4-Monomethoxytritylthio (MMTrS) Group as a 5′-Hydroxyl Protecting Group: Toward Oligonucleotide Synthesis Without Acid Treatment.;ChemInform;2010-05-22
5. Synthesis of oligodeoxynucleotides using the oxidatively cleavable 4-methoxytritylthio (MMTrS) group for protection of the 5′-hydroxyl group;New Journal of Chemistry;2010
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