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- W2103759434 abstract "Abstract We have previously described that in the crystalline structure, the five membered rings of 5-thienyl and 5-furany12′-dUrd have a different orientation according to the heteroatom involved (S or 0). NOE difference NMR experiments were conducted in order to verify this conformation in solution. A theorical conformational analysis was further computed at the “ab initio” STO-3G level, to characterize the energetic profile. This comparative study realized on some 5-heteroaromatic-2′-deoxyuridines confirms the crystallographic results." @default.
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- W2103759434 date "1997-03-01" @default.
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- W2103759434 title "Structural Study of Two 5-Heteroaromatic-2′ deoxyuridines and Their 5-Bromine-heteroaromatic Analogues: Theoretical Conformational Analysis and NMR Experiments" @default.
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- W2103759434 doi "https://doi.org/10.1080/07328319708001353" @default.
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