Mechanism of methylation of nucleoside sugar hydroxyl groups by diazomethane in the presence of stannous chloride
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference27 articles.
1. The Direct Preparation of 2'-O-Methyladenosine from Adenosine1
2. The action of diazomethane on ribonucleosides. Preparation of ribonucleoside 2'- and 3'-methyl ethers
3. Nucleic acid related compounds. II. A rapid and quantitative preparation of 2′-O- and 3′-O-methyl nucleosides
4. Nucleic acid related compounds. 12. Facileand high yield stannous chloride catalyzed monomethylation of the cis glycol system of nucleosides by diazomethane
5. Catalytic monomethylation of the cis-glycol system by diazomethane. Effects of novel inorganic catalysts on isomer ratios
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3. New evidence for the mechanism of the tin(II) chloride catalyzed reactions of vicinal diols with diazodiphenylmethane in 1,2-dimethoxyethane;Carbohydrate Research;2001-04
4. Substrate/Inhibitor Properties of Human Deoxycytidine Kinase (dCK) and Thymidine Kinases (Tk1 And Tk2) Towards the Sugar Moiety of Nucleosides, Including O′-Alkyl Analogues;Nucleosides and Nucleotides;1999-08
5. Regioselective methylation of methyl glycopyranosides with diazomethane in the presence of transition-metal chlorides and of boric acid;Carbohydrate Research;1999-03
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