Lower Rim Functionalization

Lower Rim Functionalization is the chemical modification of the phenolic hydroxyl groups positioned at the narrow circumference of a calixarene scaffold, enabling the introduction of substituents that confer tailored solubility, binding affinity, or molecular recognition properties to the macrocyclic system.

86

Publications

3.6K

Citations

329

Authors

104

Institutions

Publications per year

2017–2026

7

Authors

329

  1. DM
    D. Max Roundhill

    Texas Tech University, United States

    9 publications · 293 citations

    9

    h-index

  2. SP
    Sebastiano Pappalardo

    University of Catania, Italy

    5 publications · 242 citations

    5

    h-index

  3. KR
    Kari Rissanen

    University of Jyväskylä, Finland

    4 publications · 193 citations

    4

    h-index

  4. PE
    Paris E. Georghiou

    Memorial University of Newfoundland, Canada

    4 publications · 89 citations

    4

    h-index

  5. MF
    Melchiorre F. Parisi

    University of Messina, Italy

    4 publications · 169 citations

    4

    h-index

1–5 of 329

Venues

  1. The Journal of Organic Chemistry

    JOC · 10 publications · 585 citations

    10

    h-index

  2. Tetrahedron Letters

    7 publications · 144 citations

    7

    h-index

  3. Chemical Communications

    ChemComm · 5 publications · 82 citations

    5

    h-index

  4. Inorganic Chemistry

    5 publications · 192 citations

    5

    h-index

  5. Tetrahedron

    3 publications · 60 citations

    3

    h-index

1–5