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Volumn , Issue 19, 2003, Pages 3832-3839

Reinvestigation into the synthesis of oligonucleotides containing 5-(β-D-glucopyranosyloxymethyl)-2′-deoxyuridine

Author keywords

Ammonolysis; Decomposition; Modified nucleobase; Nucleosides; Oligonucleotides

Indexed keywords

5 (AMINOMETHYL) 2' DEOXYURIDYL DERIVATIVE; 5 (BETA DEXTRO GLUCOPYRANOSYLOXYMETHYL) 2' DEOXYURIDINE; AMMONIA; DEOXYGLUCOSE; DEOXYURIDINE DERIVATIVE; DNA FRAGMENT; OLIGONUCLEOTIDE; PHOSPHORAMIDIC ACID DERIVATIVE; UNCLASSIFIED DRUG; VARIANT SURFACE GLYCOPROTEIN;

EID: 0141891469     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/ejoc.200300218     Document Type: Article
Times cited : (18)

References (23)
  • 16
    • 0141922269 scopus 로고    scopus 로고
    • note
    • It should be noted that a higher-resolution ion-exchange column than previously was used (Dionex-Pac). In addition, the buffer was changed from pH 12 to pH 7 in order better to visualise and quantify the side product 15, which at pH 12 is a shoulder on the right hand side of the main peak (14).
  • 17
    • 0141887757 scopus 로고    scopus 로고
    • note
    • No protection of the 2-deoxyribose moiety hydroxy groups was used, as these are not responsible for decomposition and leaving them unmasked aids solubility in the aqueous medium.
  • 19
    • 0141956692 scopus 로고    scopus 로고
    • note
    • 3N· 3HF, py, room temp., 16 h
  • 20
    • 0141922267 scopus 로고    scopus 로고
    • note
    • Use of the more labile methoxyacetyl hydroxy group protection would provide no further advantage, as TAC protection requires 2 h for complete removal.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.