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Volumn 69, Issue 6, 2004, Pages 1831-1836

Ring Opening of Nucleoside 1′,2′-Epoxides with Organoaluminum Reagents: Stereoselective Entry to Ribonucleosides Branched at the Anomeric Position

Author keywords

[No Author keywords available]

Indexed keywords

ALUMINUM; DERIVATIVES; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

EID: 1642299991     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo030262u     Document Type: Article
Times cited : (47)

References (37)
  • 23
    • 0035354786 scopus 로고    scopus 로고
    • Stereoselective methods for the synthesis of ribofuranosyl uracil nucleosides have recently been reported: (a) Kodama, T.; Shuto, S.; Nomura, M.; Matsuda, A. Chem. Eur. J. 2001, 7, 2332-2340.
    • (2001) Chem. Eur. J. , vol.7 , pp. 2332-2340
    • Kodama, T.1    Shuto, S.2    Nomura, M.3    Matsuda, A.4
  • 33
    • 1642287827 scopus 로고    scopus 로고
    • note
    • The stereochemistry of epoxides derived from 2 and 9 could not be determined by NOE experiment due to their instability.
  • 34
    • 1642412868 scopus 로고    scopus 로고
    • note
    • + + H).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.