1,2-Dicarbonyl Compounds as Pronucleophiles in Organocatalytic Asymmetric Transformations - Aix-Marseille Université Access content directly
Journal Articles Angewandte Chemie International Edition Year : 2012

1,2-Dicarbonyl Compounds as Pronucleophiles in Organocatalytic Asymmetric Transformations

Wilfried Raimondi
  • Function : Author
Damien Bonne
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Jean Rodriguez
  • Function : Correspondent author
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Abstract

Organocatalysis likes them too! 1,2-dicarbonyl compounds possess high synthetic potential because of their adjacent multiple reactive centers. Recent contributions indicate that these reactive species, with an appropriate activation mode, may also act as efficient pronucleophiles in asymmetric organocatalyzed sequential or domino transformations including C-C or C-N bond formation

Dates and versions

hal-00676949 , version 1 (06-03-2012)

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Wilfried Raimondi, Damien Bonne, Jean Rodriguez. 1,2-Dicarbonyl Compounds as Pronucleophiles in Organocatalytic Asymmetric Transformations. Angewandte Chemie International Edition, 2012, 51, pp.40-42. ⟨10.1002/anie.201106741⟩. ⟨hal-00676949⟩
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