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Volumn 8, Issue 6, 2010, Pages 1445-1454

Synthesis and O-phosphorylation of 3,3,4,4-tetrafluoroaryl-C-nucleoside analogues

Author keywords

[No Author keywords available]

Indexed keywords

C-NUCLEOSIDES; ETHYLENE GROUP; PRIMARY ALCOHOLS;

EID: 77749289956     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b922442d     Document Type: Article
Times cited : (33)

References (35)
  • 28
    • 77749266414 scopus 로고    scopus 로고
    • Note
    • 2COCl, and subsequent cyclization were recently reported by Linclau et al. for ketose formations (ref. 8c)
  • 29
    • 0026029434 scopus 로고
    • For Lewis acid-promoted reductive dehydroxylation of non-fluorinated C-nucleosides, see
    • For Lewis acid-promoted reductive dehydroxylation of non-fluorinated C-nucleosides, see: J. A. Piccirilli T. Krauch L. J. MacPherson S. A. Benner Helv. Chim. Acta 1991 74 397
    • (1991) Helv. Chim. Acta , vol.74 , pp. 397
    • Piccirilli, J.A.1    Krauch, T.2    MacPherson, L.J.3    Benner, S.A.4
  • 34
    • 77749269262 scopus 로고    scopus 로고
    • Note
    • Table 3 (entries 1-3) shows the structure of the major diastereomer only; entry 1: 8a d.r.: 5:1, 9a d.r.: 5:1; entry 2: 8b d.r.: 4:1, 9b d.r.: 4:1; entry 3: 8c d.r.: 2:1, 9c d.r.: 1.4:1. For entries 4 and 5, 10d and 10e were formed as a mixture of diastereomers (d.r. = 4:1 for 10d and d.r. = 5:1 for 10e).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.