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

Wilfried Raimondi 1 Damien Bonne 1, * Jean Rodriguez 1, * 
* Corresponding author
1 STeRéO
ISM2 - Institut des Sciences Moléculaires de Marseille
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
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https://hal.archives-ouvertes.fr/hal-00676949
Contributor : Gaelle Chouraqui Connect in order to contact the contributor
Submitted on : Tuesday, March 6, 2012 - 5:35:52 PM
Last modification on : Tuesday, December 14, 2021 - 8:36:12 AM

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

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