Abstract
AbstractThis review article summarizes progress made on [1,2]-sigmatropic rearrangements using carbenes in the ylide formation step. While other rearrangements, such as the [2,3]-sigmatropic, Doyle–Kirmse, or Sommelet–Hauser rearrangements, have been studied in detail over the past decades, investigations on [1,2]-sigmatropic rearrangements are still limited. Based on the application of diazoalkanes as carbene precursors, research on diazoalkanes in ylide formation reactions started flourishing in the 1990s. This Short Review covers milestones from the advent of [1,2]-sigmatropic rearrangements using carbenes to generate ammonium, oxonium and other ylide species, and should serve as an overview to further promote research in this area.1 Introduction2 Ammonium Ylides3 Oxonium Ylides4 Sulfonium and Selenium Ylides5 Halonium Ylides6 Conclusion and Outlook
Funder
Deutsche Forschungsgemeinschaft
Fonds der Chemischen Industrie e.V.
Subject
Organic Chemistry,Catalysis
Cited by
20 articles.
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