An Efficient Process for Synthesis of 2′-O-methyl and 3′-O-methyl Guanosine from 2-aminoadenosine Using Diazomethane and the Catalyst Stannous Chloride

AR Kore, G Parmar, S Reddy

Index: Nucleosides, Nucleotides and Nucleic Acids, , vol. 25, # 3 p. 307 - 314

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Citation Number: 7

Abstract

... methoxy-2-pyrimidinone 1-β -D-ribofuranoside into 2′-O-methyl nucleoside components of ... stannous chloride catalyzed monomethylation of the cis-glycol system of nucleosides by diazomethane ... for the simultaneous protection of the 3′ and 5′ hydroxyl groups of nucleotides. ...

An Efficient Process for Synthesis of 2′-O-methyl and 3′-O-methyl Guanosine from 2-aminoadenosine Using Diazomethane and the Catalyst Stannous Chloride

[Kore, Anilkumar; Parmar, Gaurang; Reddy, Srinu Nucleosides, Nucleotides and Nucleic Acids, 2006 , vol. 25, # 3 p. 307 - 314]

Nucleic Acid Related Compounds. 36. Synthesis of the 2'-O-methyl and 3'-O-methyl Ethers of Guanosine and 2-Aminoadenosine and Correlation of O'- …

[Canadian Journal of Chemistry, , vol. 59, p. 3360 - 3364]

An Efficient Process for Synthesis of 2′-O-methyl and 3′-O-methyl Guanosine from 2-aminoadenosine Using Diazomethane and the Catalyst Stannous Chloride

Abstract

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