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Volumn 62, Issue 46, 2006, Pages 10694-10699

Dye-sensitized photooxygenation of sugar-furans as synthetic strategy for novel C-nucleosides and functionalized exo-glycals

Author keywords

1,3 Dipolar cycloadditions; 4+2 Cycloadditions; C Nucleosides; Photooxygenation

Indexed keywords

1,3 DIOXANE DERIVATIVE; C NUCLEOSIDE; CARBOHYDRATE DERIVATIVE; FURAN DERIVATIVE; METHYLENE BLUE; PYRAZOLINE DERIVATIVE; PYRIDAZINE DERIVATIVE;

EID: 33749316925     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2006.07.109     Document Type: Article
Times cited : (19)

References (34)
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  • 32
    • 33749352848 scopus 로고    scopus 로고
    • note
    • The β-anomer 1e was the main product (β:α=8:1) owing to the neighbouring group of the acetyl at C-2 of the glycosyl donor.
  • 33
    • 85077874503 scopus 로고
    • Diacetylethylenes may undergo polymerization, mainly on contact with chromatographic adsorbents ( )
    • Diacetylethylenes may undergo polymerization, mainly on contact with chromatographic adsorbents (. Graziano M.L., Iesce M.R., and Scarpati R. Synthesis (1983) 125 )
    • (1983) Synthesis , pp. 125
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    • note
    • High equivalents of the reactants were used to balance those oxidating diethyl sulfoxide present in the crude reaction mixture.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.