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Volumn 9, Issue 16, 2007, Pages 3057-3060

Syntheses of (2′)3′-15N/-Amino-(2′)3′- deoxyguanosine and determination of Their pKa values by15N NMR spectroscopy

Author keywords

[No Author keywords available]

Indexed keywords

DEOXYGUANOSINE; DRUG DERIVATIVE; RIBOZYME;

EID: 34547936757     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol071129h     Document Type: Article
Times cited : (7)

References (52)
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    • Persson, T.; S. C.; Hartmann, R. K. J. Biol. Chem. 2003, 278, 43394.
    • Persson, T.; S. C.; Hartmann, R. K. J. Biol. Chem. 2003, 278, 43394.
  • 38
    • 34547944852 scopus 로고
    • Jpn. Kokai Tokkyo Koho, JP, 60228497, A2, 19851113
    • Ishida, N.; Tanaka, T.; Atami, T. Jpn. Kokai Tokkyo Koho 1985, JP, 60228497, A2, 19851113.
    • (1985)
    • Ishida, N.1    Tanaka, T.2    Atami, T.3
  • 41
    • 34547952156 scopus 로고    scopus 로고
    • 15N-labeled benzylamine.
    • 15N-labeled benzylamine.
  • 43
    • 34547940582 scopus 로고    scopus 로고
    • When THF was used as solvent, 2a failed to give desired product 2b.
    • When THF was used as solvent, 2a failed to give desired product 2b.
  • 48
    • 34547949047 scopus 로고    scopus 로고
    • In the report from Zhang et al.,25 the 5′-TBDPS silyl protecting group was also removed in this step. However, under the same reaction conditions, the protecting group survived in our experiments
    • 25 the 5′-TBDPS silyl protecting group was also removed in this step. However, under the same reaction conditions, the protecting group survived in our experiments.
  • 49
    • 34547939778 scopus 로고    scopus 로고
    • The following buffers were used: sodium acetate, pH 4.5-5.50; NaMES, pH 5.75-6.50; NaMOPS, pH 6.75-7.50; NaEPPS, pH 7.75-8.50; NaCHES, pH 9.0-9.5.
    • The following buffers were used: sodium acetate, pH 4.5-5.50; NaMES, pH 5.75-6.50; NaMOPS, pH 6.75-7.50; NaEPPS, pH 7.75-8.50; NaCHES, pH 9.0-9.5.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.