3,4-etheno-5-methoxymethyl-2′-deoxycytidine

Gerald F. Audette, Wajdi M. Zoghaib, Guy Tourigny, Sagar V. Gupta, Louis T J Delbaere

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

In the title compound, C13H17N3O5, the deoxyribose sugar ring adopts a C2′-exo-C3′-endo symmetrical half-chair conformation (23T), with pseudorotational parameters of P = 2.54 (1)° and τm = 27.82 (7)°. The deoxyribose sugar ring is in the anticlinal (-ac) conformation with respect to the base [x = -93.2 (4)°]. The exocyclic side chain at C5′ is in the gg conformation [γ = 57.2 (3)°]. The methoxymethyl side chain at C5 is oriented towards the exocyclic side chain at C5′.

Original languageEnglish
Pages (from-to)1099-1101
Number of pages3
JournalActa Crystallographica Section C: Crystal Structure Communications
Volume53
Issue number8
Publication statusPublished - Aug 15 1997

ASJC Scopus subject areas

  • Condensed Matter Physics
  • Structural Biology

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  • Cite this

    Audette, G. F., Zoghaib, W. M., Tourigny, G., Gupta, S. V., & Delbaere, L. T. J. (1997). 3,4-etheno-5-methoxymethyl-2′-deoxycytidine. Acta Crystallographica Section C: Crystal Structure Communications, 53(8), 1099-1101.