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Volumn 13, Issue 15, 2003, Pages 2441-2443

Convenient synthesis of oligodeoxyribonucleotides bearing arabinofuranosyl pyrimidine derivatives and its duplex formation with complementary DNA

Author keywords

[No Author keywords available]

Indexed keywords

ARABINOFURANOSE; ARABINOSE; COMPLEMENTARY DNA; DRUG DERIVATIVE; DYES, REAGENTS, INDICATORS, MARKERS AND BUFFERS; OLIGODEOXYRIBONUCLEOTIDE; PYRIMIDINE DERIVATIVE;

EID: 0038309327     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-894X(03)00500-6     Document Type: Article
Times cited : (9)

References (17)
  • 10
    • 0028286623 scopus 로고
    • Arabinoaminooxazoline allowed to react with ethyl α-(bromomethyl)-acrylate and the product was treated with potassium t-butoxide. Ref.;
    • Arabinoaminooxazoline allowed to react with ethyl α-(bromomethyl)-acrylate and the product was treated with potassium t-butoxide. Ref.; Sawai H., Nakamura A., Hayashi H., Shinozuka K. Nucleosides and Nucleotides. 13:1994;1647.
    • (1994) Nucleosides and Nucleotides , vol.13 , pp. 1647
    • Sawai, H.1    Nakamura, A.2    Hayashi, H.3    Shinozuka, K.4
  • 12
    • 85031155505 scopus 로고    scopus 로고
    • + 387.2, found 387.3.
  • 14
    • 85031155504 scopus 로고    scopus 로고
    • For example, 1a in addition of four natural deoxynucleosides was detected on HPLC when ODN4a, which was identified by ESI-MS, was degraded by nucleases (snake venom phosphodiesterase, nuclease P1, and alkaline phophatase).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.