• Title of article

    Conformational studies of the linear homooligomers of a glucose-derived furanoid sugar amino acid

  • Author/Authors

    Chakraborty، نويسنده , , Tushar K and Srinivasu، نويسنده , , P and Sakunthala Madhavendra، نويسنده , , S and Kiran Kumar، نويسنده , , S and Kunwar، نويسنده , , Ajit C، نويسنده ,

  • Issue Information
    هفته نامه با شماره پیاپی سال 2004
  • Pages
    5
  • From page
    3573
  • To page
    3577
  • Abstract
    Conformational analysis of the linear tetramer of the glucose-derived furanoid sugar amino acid 1 by NMR and constrained molecular dynamics studies revealed that the fully protected tetramer 2a has a well-defined structure in CDCl3 with repeating β-turns, each involving a 10-membered ring structure with intramolecular hydrogen bonds between NHi → COi−2. Its deprotected versions 2b and 2c showed aggregation in organic solvents with structures similar to that of 2a.
  • Keywords
    Sugar amino acids , Oligomer , NMR , Hydrogen bonding , Conformation
  • Journal title
    Tetrahedron Letters
  • Serial Year
    2004
  • Journal title
    Tetrahedron Letters
  • Record number

    1841449