Exo-anomeric Effect

The Exo-Anomeric Effect is a stereoelectronic phenomenon in carbohydrate chemistry wherein the preference for a specific orientation of the lone pair on the ring oxygen relative to the exocyclic C–O bond at the anomeric center stabilizes the molecular conformation through hyperconjugative interactions.

97

Publications

4K

Citations

292

Authors

113

Institutions

Publications per year

2017–2026

9

Variants

Exoanomeric Effect

Authors

292

  1. IT
    Igor Tvaroška

    Slovak Academy of Sciences, Slovakia

    6 publications · 185 citations

    6

    h-index

  2. JJ
    Jesús Jiménez‐Barbero

    Centro de Investigaciones Biológicas Margarita Salas, Spain

    5 publications · 164 citations

    5

    h-index

  3. JT
    Jesús Téllez Vázquez

    Universidad de La Laguna, Spain

    4 publications · 113 citations

    4

    h-index

  4. CJ
    Christopher J. Cramer

    University of Minnesota, United States

    3 publications · 252 citations

    3

    h-index

  5. NP
    Normand Pothier

    Université de Sherbrooke, Canada

    3 publications · 180 citations

    3

    h-index

1–5 of 292

Venues

  1. Carbohydrate Research

    11 publications · 566 citations

    11

    h-index

  2. The Journal of Organic Chemistry

    JOC · 10 publications · 298 citations

    10

    h-index

  3. Tetrahedron

    9 publications · 361 citations

    9

    h-index

  4. Canadian Journal of Chemistry

    8 publications · 856 citations

    8

    h-index

  5. Journal of the American Chemical Society

    JACS · 6 publications · 275 citations

    6

    h-index

1–5