Stereochemical Inversion

Stereochemical Inversion is a stereochemical process in which the spatial arrangement of atoms around a chiral center in a herbicide molecule is reversed, leading to the conversion of one enantiomer into its mirror-image counterpart, thereby potentially altering its biological activity, environmental fate, and selectivity in target and non-target organisms.

386

Publications

16.9K

Citations

1.2K

Authors

297

Institutions

Publications per year

2017–2026

23

Authors

1.2K

  1. JC
    Jonathan Clayden

    University of Manchester, United Kingdom

    6 publications · 217 citations

    6

    h-index

  2. GB
    G. BERNÁTH

    University of Szeged, Hungary

    5 publications · 128 citations

    5

    h-index

  3. PS
    Pàl Sohár

    University of Szeged, Hungary

    5 publications · 114 citations

    5

    h-index

  4. JS
    J. Sicher

    Czech Academy of Sciences, Institute of Organic Chemistry and Biochemistry, Czechia

    4 publications · 49 citations

    4

    h-index

  5. KM
    Kurt Mislow

    Princeton University, United States

    4 publications · 85 citations

    4

    h-index

1–5 of 1.2K

Venues

  1. Journal of the American Chemical Society

    JACS · 59 publications · 3.3K citations

    33

    h-index

  2. Tetrahedron Letters

    30 publications · 804 citations

    20

    h-index

  3. Tetrahedron

    31 publications · 1.2K citations

    19

    h-index

  4. Angewandte Chemie International Edition

    15 publications · 1.7K citations

    15

    h-index

  5. The Journal of Organic Chemistry

    JOC · 18 publications · 638 citations

    14

    h-index

1–5