Synthesis of C-Ribo-nucleosides Having Typical Aromatic Heterocycles as Base Moiety
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概要
- 論文の詳細を見る
- 1994-02-05
著者
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TOGO Hideo
Department of Chemistry, Faculty of Science, Chiba University
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Akiba Takahiro
Department Of Chemistry Faculty Of Science Chiba University
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Togo Hideo
Department Of Chemistry Faculty Of Science Chiba University
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YOKOHAMA Masataka
Department of Chemistry, Faculty of Science, Chiba University
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TOYOSHIMA Akira
Department of Chemistry, Faculty of Science, Chiba University
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Toyoshima Akira
Department Of Chemistry Faculty Of Science Chiba University
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Yokohama Masataka
Department Of Chemistry Faculty Of Science Chiba University
関連論文
- Novel Degradation of Sugar Skeleton by Diazidation
- Thermolysis and Photolysis of Sugar Diazides
- A Facile Preparative Method of C-Nucleosides
- Synthesis of Pyrrole Derivatives Using Thioimidates
- Novel Water-Soluble Organosilane Compounds as a Radical Reducing Agent in Aqueous Media
- Alkylation of Heteroaromatic Bases with Diphenylselenium Diacyloxylate
- Synthesis of C-Ribo-nucleosides Having Typical Aromatic Heterocycles as Base Moiety
- Reductive Addition of Alkyl Radical to Phenyl Vinyl Sulfone
- Tris(trimethylsily)silane in the Alkylation of Heteroaromatic Bases with Alkyl Halides
- Conversion of hydroxyl groups in alcohols to other functional groups witn N-hydroxy-2-thiopyridone, and its application to dialkylamines and thiols.