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Volumn 15, Issue 24, 1974, Pages 2141-2144

Nucleosides, XX. Stannic chloride catalyzed glycosidations of silylated purines with fully acylated sugars

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EID: 0013109206     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(01)82653-8     Document Type: Article
Times cited : (58)

References (23)
  • 2
    • 84980182647 scopus 로고
    • Studies on Nucleosides and Nucleotides. VII-VIII. VII. A New Method for Synthesis of Purine-Ribonucleosides. Part. 1
    • (1961) Nippon kagaku zassi , vol.81 , pp. 1440
    • Sato1    Shimadate2    Ishido3
  • 3
    • 84914646979 scopus 로고
    • Studies on Nucleosides and Nucleotides. VII-VIII. VIII. A N ew Method for Synthesis of Purine-Ribonucleosides, . Part. 2
    • (1961) Nippon kagaku zassi , vol.81 , pp. 1442
    • Sato1    Shimadate2    Ishido3
  • 11
    • 0014094683 scopus 로고
    • The chloromercury derivative of 2-acetamido-6-chloropurine gave unsatisfactory results
    • (1967) J. Org. Chem. , vol.32 , pp. 1984
    • Tong1    Lee2    Goodman3
  • 15
    • 84918306611 scopus 로고
    • Studies on Synthetic Nucleosides
    • Trimethylsilyl-purines have only been used in glycosidations with acylglycosyl halides (fusion at 150–160°), giving α, β-anomeric mixtures that require column chromatography for separations
    • (1964) Agricultural and Biological Chemistry , vol.28 , pp. 224
    • Nishimura1
  • 18
    • 79851469452 scopus 로고
    • Allgemeine Synthese von Pyrimidin-nucleosiden
    • These are standard conditions for N-glycosidations of silylated pyrimidines with 1-O-acylglycoses, ref. 1 and other literature cited there.
    • (1970) Angewandte Chemie , vol.82 , pp. 449
    • Niedballa1    Vorbrüggen2
  • 19
    • 84918303264 scopus 로고    scopus 로고
    • 4b.
  • 22
    • 84918303263 scopus 로고    scopus 로고
    • max 250 nm (dioxan) by refluxing pyrazolo[3, 4-d]pyrimidin-4-one (allopurinol) in hexamethyldisilanzane.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.