E1cb Elimination

E1cb Elimination is an elimination reaction mechanism characterized by a stepwise process in which the departure of a leaving group follows the initial formation of a stabilized carbanion intermediate, distinguishing it from other elimination pathways by its carbanion-mediated kinetics and strong dependence on substrate acidity.

58

Publications

1.8K

Citations

181

Authors

58

Institutions

Publications per year

2017–2026

9

Variants

E1cb MechanismUnimolecular Conjugate Base Elimination

Authors

181

  1. SA
    Sergio Alunni

    University of Perugia, Italy

    6 publications · 143 citations

    6

    h-index

  2. AT
    Alf Thibblin

    Uppsala University, Sweden

    4 publications · 83 citations

    4

    h-index

  3. RA
    Rory A. More O‘Ferrall

    University College Dublin, Ireland

    3 publications · 274 citations

    3

    h-index

  4. ÉD
    Éric Deniau

    Laboratoire de Chimie Organique, France

    3 publications · 166 citations

    3

    h-index

  5. AC
    Axel Couture

    Laboratoire de Chimie Organique, France

    3 publications · 166 citations

    3

    h-index

1–5 of 181

Venues

  1. Journal of the American Chemical Society

    JACS · 15 publications · 445 citations

    13

    h-index

  2. The Journal of Organic Chemistry

    JOC · 11 publications · 312 citations

    10

    h-index

  3. 7

    h-index

  4. Organic & Biomolecular Chemistry

    5 publications · 152 citations

    5

    h-index

  5. 3

    h-index

1–5