메뉴 건너뛰기




Volumn 55, Issue 17, 1999, Pages 5319-5344

Face selective 6,1'-(1-oxo)ethano bridge formation of uracil nucleosides under hypoiodite reaction conditions

Author keywords

[No Author keywords available]

Indexed keywords

PYRIMIDINE NUCLEOTIDE;

EID: 0033597355     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(99)00232-X     Document Type: Article
Times cited : (12)

References (53)
  • 3
    • 12044260107 scopus 로고
    • (c) Goldberg, I. H. Acc. Chem. Res. 1991, 24, 191-198.
    • (1991) Acc. Chem. Res. , vol.24 , pp. 191-198
  • 4
  • 9
    • 0032557199 scopus 로고    scopus 로고
    • α-Anomerization of deoxyadenosine by hydroxyl radicals in DNA
    • (i) Chen, T.; Greenberg, M. M. J. Am. Chem. Soc. 1998, 120, 3815-3816. α-Anomerization of deoxyadenosine by hydroxyl radicals in DNA:
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 3815-3816
    • Chen, T.1    Greenberg, M.M.2
  • 19
    • 0001057597 scopus 로고    scopus 로고
    • Anomeric radical formation of Norrish type I photoprocess
    • (g) Gimisis, T.; Chatgilialoglu, C. J. Org. Chem. 1996, 61, 1908-1909. Anomeric radical formation of Norrish type I photoprocess:
    • (1996) J. Org. Chem. , vol.61 , pp. 1908-1909
    • Gimisis, T.1    Chatgilialoglu, C.2
  • 28
    • 84987559681 scopus 로고
    • (b) For leading references, see: Heusler, K; Kalvoda, J. Angew. Chem., Int. Ed. Engl. 1964, 3, 525-59; Kalvoda, J.; Heusler, K. Synthesis 1971, 501-526.
    • (1971) Synthesis , pp. 501-526
    • Kalvoda, J.1    Heusler, K.2
  • 42
    • 0013542611 scopus 로고    scopus 로고
    • For convenience, β-spiro nucleosides describe the anomeric stereochemistry in which the base moiety occupies the same face as the 4′-hydroxymethyl group.
    • 7. For convenience, β-spiro nucleosides describe the anomeric stereochemistry in which the base moiety occupies the same face as the 4′-hydroxymethyl group.
  • 51
    • 0013518368 scopus 로고    scopus 로고
    • note
    • 3/MeOH). To some extent, deacetylation occurred during the subsequent acidic treatment; and the 2′,3′,5′-tris-O-silylation step was also problematic in this sequence.
  • 53
    • 0013477498 scopus 로고    scopus 로고
    • Possibility of C7-alkoxy radical formation from the C1'-iodo intermediate iv with excess reagents followed by radical substitution reaction on the anomeric carbon for cyclization would also be considered
    • 14. Possibility of C7-alkoxy radical formation from the C1'-iodo intermediate iv with excess reagents followed by radical substitution reaction on the anomeric carbon for cyclization would also be considered.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.