Nucleobase Aromaticity

Nucleobase Aromaticity is a physicochemical property characterized by the delocalization of π-electrons within the heterocyclic ring systems of nucleobases, conferring enhanced stability, planarity, and characteristic electronic absorption that distinguishes aromatic nucleobases from non-aromatic analogues in the context of nucleic acid structure and reactivity.

89

Publications

4K

Citations

320

Authors

117

Institutions

Publications per year

2017–2026

8

Authors

320

  1. BL
    Bernhard Lippert

    TU Dortmund University, Germany

    12 publications · 500 citations

    12

    h-index

  2. JC
    Jyoti Chattopadhyaya

    Uppsala University, Sweden

    4 publications · 108 citations

    4

    h-index

  3. UT
    Ulf Thewalt

    Universität Ulm, Germany

    4 publications · 249 citations

    4

    h-index

  4. PA
    Parag Acharya

    Uppsala University, Sweden

    3 publications · 85 citations

    3

    h-index

  5. SA
    Sandipta Acharya

    Uppsala University, Sweden

    3 publications · 85 citations

    3

    h-index

1–5 of 320

Venues

  1. Journal of the American Chemical Society

    JACS · 12 publications · 807 citations

    12

    h-index

  2. The Journal of Physical Chemistry A

    6 publications · 225 citations

    7

    h-index

  3. Inorganic Chemistry

    5 publications · 145 citations

    5

    h-index

  4. The Journal of Physical Chemistry B

    4 publications · 279 citations

    4

    h-index

  5. Tetrahedron Letters

    3 publications · 59 citations

    3

    h-index

1–5