Matches in SemOpenAlex for { <https://semopenalex.org/work/W2147273886> ?p ?o ?g. }
Showing items 1 to 86 of
86
with 100 items per page.
- W2147273886 endingPage "346" @default.
- W2147273886 startingPage "343" @default.
- W2147273886 abstract "The preparation and high-resolution 1H NMR conformational analysis of the two novel nucleoside analogues, 1-(3′-C-methyl-2′-deoxy-β-D-xylofuranosyl)uracil (compound 1) and 9-(3′-C-methyl-2′-deoxy-β-D-xylofuranosyl)adenine (compound 2), are described. Compounds 1 and 2 show a pronounced preference for the north conformation of the sugar ring. The north conformation corresponds with a sterically favoured equatorial location of the methyl group. The C4′ - C5′ conformation in 1 and 2 is predominantly γt (trans orientation of O5′ and C3′). The configuration at C3′ in 1 and 2 was corroborated via a one-dimensional NOE experiment. The structure of compound 1 (originally assigned as having the C3′-methyl group on the β-face of the furanosyl moiety) is revised on the basis of these data." @default.
- W2147273886 created "2016-06-24" @default.
- W2147273886 creator A5008210963 @default.
- W2147273886 creator A5033599043 @default.
- W2147273886 creator A5056056233 @default.
- W2147273886 creator A5063027392 @default.
- W2147273886 creator A5068711541 @default.
- W2147273886 creator A5077819364 @default.
- W2147273886 creator A5078839283 @default.
- W2147273886 date "2010-09-02" @default.
- W2147273886 modified "2023-09-25" @default.
- W2147273886 title "Synthesis and conformation of 1-(3′-C-methyl-2′-deoxy-β-D-xylofuranosyl)uracil and 9-(3′-C-methyl-2′-deoxy-β-D-xylofuranosyl)adenine; two novel sugar-methylated nucleoside analogues" @default.
- W2147273886 cites W1483413211 @default.
- W2147273886 cites W1972877409 @default.
- W2147273886 cites W2014385381 @default.
- W2147273886 cites W2024805770 @default.
- W2147273886 cites W2028626711 @default.
- W2147273886 cites W2040653354 @default.
- W2147273886 cites W2061822610 @default.
- W2147273886 cites W2073134966 @default.
- W2147273886 cites W2085024742 @default.
- W2147273886 cites W2090955661 @default.
- W2147273886 cites W2098001281 @default.
- W2147273886 cites W2157147320 @default.
- W2147273886 cites W53123824 @default.
- W2147273886 doi "https://doi.org/10.1002/recl.19881070408" @default.
- W2147273886 hasPublicationYear "2010" @default.
- W2147273886 type Work @default.
- W2147273886 sameAs 2147273886 @default.
- W2147273886 citedByCount "20" @default.
- W2147273886 countsByYear W21472738862013 @default.
- W2147273886 crossrefType "journal-article" @default.
- W2147273886 hasAuthorship W2147273886A5008210963 @default.
- W2147273886 hasAuthorship W2147273886A5033599043 @default.
- W2147273886 hasAuthorship W2147273886A5056056233 @default.
- W2147273886 hasAuthorship W2147273886A5063027392 @default.
- W2147273886 hasAuthorship W2147273886A5068711541 @default.
- W2147273886 hasAuthorship W2147273886A5077819364 @default.
- W2147273886 hasAuthorship W2147273886A5078839283 @default.
- W2147273886 hasConcept C178790620 @default.
- W2147273886 hasConcept C185592680 @default.
- W2147273886 hasConcept C201194858 @default.
- W2147273886 hasConcept C2776543447 @default.
- W2147273886 hasConcept C2776568683 @default.
- W2147273886 hasConcept C2777108408 @default.
- W2147273886 hasConcept C2778565081 @default.
- W2147273886 hasConcept C2779554091 @default.
- W2147273886 hasConcept C2780378348 @default.
- W2147273886 hasConcept C2781311116 @default.
- W2147273886 hasConcept C552990157 @default.
- W2147273886 hasConcept C55493867 @default.
- W2147273886 hasConcept C71240020 @default.
- W2147273886 hasConceptScore W2147273886C178790620 @default.
- W2147273886 hasConceptScore W2147273886C185592680 @default.
- W2147273886 hasConceptScore W2147273886C201194858 @default.
- W2147273886 hasConceptScore W2147273886C2776543447 @default.
- W2147273886 hasConceptScore W2147273886C2776568683 @default.
- W2147273886 hasConceptScore W2147273886C2777108408 @default.
- W2147273886 hasConceptScore W2147273886C2778565081 @default.
- W2147273886 hasConceptScore W2147273886C2779554091 @default.
- W2147273886 hasConceptScore W2147273886C2780378348 @default.
- W2147273886 hasConceptScore W2147273886C2781311116 @default.
- W2147273886 hasConceptScore W2147273886C552990157 @default.
- W2147273886 hasConceptScore W2147273886C55493867 @default.
- W2147273886 hasConceptScore W2147273886C71240020 @default.
- W2147273886 hasIssue "4" @default.
- W2147273886 hasLocation W21472738861 @default.
- W2147273886 hasOpenAccess W2147273886 @default.
- W2147273886 hasPrimaryLocation W21472738861 @default.
- W2147273886 hasRelatedWork W1967112308 @default.
- W2147273886 hasRelatedWork W1989616250 @default.
- W2147273886 hasRelatedWork W2023175960 @default.
- W2147273886 hasRelatedWork W2037384651 @default.
- W2147273886 hasRelatedWork W2051870095 @default.
- W2147273886 hasRelatedWork W2055249750 @default.
- W2147273886 hasRelatedWork W2077857494 @default.
- W2147273886 hasRelatedWork W2949694875 @default.
- W2147273886 hasRelatedWork W2949730139 @default.
- W2147273886 hasRelatedWork W3172971902 @default.
- W2147273886 hasVolume "107" @default.
- W2147273886 isParatext "false" @default.
- W2147273886 isRetracted "false" @default.
- W2147273886 magId "2147273886" @default.
- W2147273886 workType "article" @default.