메뉴 건너뛰기




Volumn 63, Issue 17, 2007, Pages 3515-3527

Furan decorated nucleoside analogues as fluorescent probes: synthesis, photophysical evaluation, and site-specific incorporation

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; DEOXYURIDINE; FLUORESCENT DYE; FURAN; NUCLEOSIDE ANALOG; OLIGONUCLEOTIDE; PURINE; PYRIMIDINE;

EID: 33947229382     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2007.01.073     Document Type: Article
Times cited : (125)

References (58)
  • 49
    • 33947255494 scopus 로고    scopus 로고
    • It has been shown that conjugation of a thiophene or thiazole moiety to the 6-position of guanosine results in highly fluorescent nucleoside analogues, for details see: Mitsui, T.; Kimoto, M.; Kawai, R.; Yokoyama, S.; Hirao, I. Tetrahedron, in press. doi:10.1016/j.tet.2006.11.096
  • 52
    • 33947288489 scopus 로고    scopus 로고
    • note
    • The ribose forms of adenosine and guanosine were used due to their commercial availability.
  • 56
    • 33947194772 scopus 로고    scopus 로고
    • note
    • Adequate fluorescence readings also depend upon the sensitivity of the luminescence spectrometer.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.