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Volumn , Issue 19, 2009, Pages 3265-3271

Improved synthesis and isolation of 2'-O-methyladenosine: Effective and scalable enzymatic separation of 2'/3'-O-methyladenosine regioisomers

Author keywords

Acylation; Enzymes; Green chemistry; Isomers; Nucleosides; Separation of isomers

Indexed keywords


EID: 67650891592     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.200900348     Document Type: Article
Times cited : (17)

References (47)
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    • For recent accounts on 2'-O-methylation of guanosine and adenosine, see: a A. R. Kore, G. Parmar, S. Reddy, Nucleosides Nucleotides Nucleic Acids 2006, 25, 307-314;
    • For recent accounts on 2'-O-methylation of guanosine and adenosine, see: a) A. R. Kore, G. Parmar, S. Reddy, Nucleosides Nucleotides Nucleic Acids 2006, 25, 307-314;
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    • For comprehensive literature, see:, Eds: S. L. Beaucage, D. E. Bergstrom, G. D. Glick, R. A. Jones, John Wiley & Sons, New York, chapter 2;
    • a) For comprehensive literature, see: Current Protocols in Nucleic Acid Chemistry (Eds: S. L. Beaucage, D. E. Bergstrom, G. D. Glick, R. A. Jones), John Wiley & Sons, New York, 2007, chapter 2;
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    • I. Lavandera, J. García, S. Fernández, M. Ferrero, V. Gotor, Y. S. Sanghvi, in Current Protocols in Nucleic Acid Chemistry, (Eds: S. L. Beaucage, D. E. Bergstrom, G. D. Glick, R. A. Jones), John Wiley & Sons, New York, 2005, chapter 2, pp. 2.11.1-2.11.36.
    • I. Lavandera, J. García, S. Fernández, M. Ferrero, V. Gotor, Y. S. Sanghvi, in Current Protocols in Nucleic Acid Chemistry, (Eds: S. L. Beaucage, D. E. Bergstrom, G. D. Glick, R. A. Jones), John Wiley & Sons, New York, 2005, chapter 2, pp. 2.11.1-2.11.36.
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    • The equimolar mixture of the two nucleosides was prepared by mixing the equal weight of 2'-0-methyladenosine (1) and 3'O-methyladenosine (2) with an intention of giving both nucleosides an equal chance to compete for enzymatic acylation process.
    • The equimolar mixture of the two nucleosides was prepared by mixing the equal weight of 2'-0-methyladenosine (1) and 3'O-methyladenosine (2) with an intention of giving both nucleosides an equal chance to compete for enzymatic acylation process.
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    • Presence of about 3% of starting material 1 was confirmed along with 97% of compound 3 in the HPLC analysis.
    • Presence of about 3% of starting material 1 was confirmed along with 97% of compound 3 in the HPLC analysis.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.