Exoanomeric Effect

The exoanomeric effect is a stereoelectronic phenomenon in carbohydrate conformation whereby the preference for a specific orientation of the exocyclic C–O bond at the anomeric center arises due to hyperconjugative stabilization between the lone pair on the ring oxygen and the antibonding orbital of the adjacent C–O bond.

27

Publications

1.3K

Citations

80

Authors

40

Institutions

Publications per year

2017–2026

2

Variants

Exo-anomeric Effect

Publications

27

1–5 of 27

Authors

80

  1. IT
    Igor Tvaroška

    Slovak Academy of Sciences, Slovakia

    5 publications · 219 citations

    5

    h-index

  2. TK
    Tibor Kožár

    Slovak Academy of Sciences, Slovakia

    2 publications · 107 citations

    2

    h-index

  3. RH
    R. H. Marchessault

    McGill University, Canada

    2 publications · 127 citations

    2

    h-index

  4. TB
    Tomáš Bleha

    Polymer Institute of the Slovak Academy of Sciences, Slovakia

    2 publications · 98 citations

    2

    h-index

  5. KA
    Khedhair A. Khedhair

    University of Nottingham, United Kingdom

    2 publications · 81 citations

    2

    h-index

1–5 of 80

Venues

  1. Carbohydrate Research

    8 publications · 544 citations

    8

    h-index

  2. Journal of the American Chemical Society

    JACS · 3 publications · 261 citations

    3

    h-index

  3. Canadian Journal of Chemistry

    3 publications · 122 citations

    3

    h-index

  4. 3

    h-index

  5. Journal of Biological Chemistry

    JBC · 1 publications · 65 citations

    1

    h-index

1–5