Wittig Reaction

The Wittig Reaction is an organic chemical reaction in which an aldehyde or ketone undergoes nucleophilic addition with a phosphonium ylide to form an alkene, distinguished by the formation of a carbon–carbon double bond through the transformation of a carbonyl group into a vinyl group.

2.7K

Publications

98.7K

Citations

7.4K

Authors

1.2K

Institutions

Publications per year

2017–2026

204

Variants

Wittig Olefination

Authors

7.4K

  1. SW
    Stuart Warren

    University of Cambridge, United Kingdom

    24 publications · 855 citations

    20

    h-index

  2. MD
    Ming‐Wu Ding

    Central China Normal University, China

    34 publications · 793 citations

    19

    h-index

  3. WL
    Wenwei Lin

    National Taiwan Normal University, Taiwan

    22 publications · 820 citations

    18

    h-index

  4. AR
    Ali Ramazani

    University of Zanjan, Iran

    18 publications · 753 citations

    17

    h-index

  5. FP
    Francisco Palácios

    University of the Basque Country, Spain

    19 publications · 1.2K citations

    17

    h-index

1–5 of 7.4K

Venues

  1. Journal of the American Chemical Society

    JACS · 111 publications · 9K citations

    60

    h-index

  2. The Journal of Organic Chemistry

    JOC · 298 publications · 12.2K citations

    58

    h-index

  3. Organic Letters

    OL · 126 publications · 5.7K citations

    48

    h-index

  4. Tetrahedron Letters

    260 publications · 7.3K citations

    40

    h-index

  5. Synthesis

    121 publications · 4.6K citations

    35

    h-index

1–5