Synthesis and structures of deoxyribonucleoside analogues for triazole-linked DNA ( super(TL)DNA)
Deoxyribonucleoside analogues bearing acetylene group at the pseudo-5'-position and azido group at the pseudo-3'-position have been synthesized by transglycosylation reaction of deoxythymidine analogue with adenine, cytosine, and guanine nucleobases as nucleophiles. The structures of analo...
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Veröffentlicht in: | Tetrahedron letters 2010-04, Vol.51 (15), p.2036-2038 |
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creator | Fujino, Tomoko Tsunaka, Nobuhide Guillot-Nieckowski, Marine Nakanishi, Waka Iwamoto, Takeaki Nakamura, Eiichi Isobe, Hiroyuki |
description | Deoxyribonucleoside analogues bearing acetylene group at the pseudo-5'-position and azido group at the pseudo-3'-position have been synthesized by transglycosylation reaction of deoxythymidine analogue with adenine, cytosine, and guanine nucleobases as nucleophiles. The structures of analogues were studied in crystalline state by X-ray crystallography as well as in solution phase by NMR spectroscopy and showed the puckering conformations similar to the natural congeners. AB: |
doi_str_mv | 10.1016/j.tetlet.2010.02.046 |
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The structures of analogues were studied in crystalline state by X-ray crystallography as well as in solution phase by NMR spectroscopy and showed the puckering conformations similar to the natural congeners. 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The structures of analogues were studied in crystalline state by X-ray crystallography as well as in solution phase by NMR spectroscopy and showed the puckering conformations similar to the natural congeners. 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The structures of analogues were studied in crystalline state by X-ray crystallography as well as in solution phase by NMR spectroscopy and showed the puckering conformations similar to the natural congeners. AB:</abstract><doi>10.1016/j.tetlet.2010.02.046</doi><tpages>3</tpages></addata></record> |
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title | Synthesis and structures of deoxyribonucleoside analogues for triazole-linked DNA ( super(TL)DNA) |
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