Enantioselective Organocatalytic Four-Atom Ring Expansion of Cyclobutanones: Synthesis of Benzazocinones - Aix-Marseille Université Accéder directement au contenu
Article Dans Une Revue Angewandte Chemie International Edition Année : 2019

Enantioselective Organocatalytic Four-Atom Ring Expansion of Cyclobutanones: Synthesis of Benzazocinones

Résumé

An enantioselective Michael addition-four-atom ring expansion cascade reaction involving cyclobutanones activated by a N-aryl secondary amide group and ortho-amino nitrostyrenes has been developed for the preparation of functionalized eight-membered benzolactams using bifunc-tional aminocatalysts. Taking advantage of the secondary amide activating group, the eight-membered cyclic products could be further rearranged into their six-membered isomers having a glutarimide core under base catalysis conditions without erosion of optical purity, featuring an overall ring expansion-ring contraction strategy.
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Dates et versions

hal-02331607 , version 1 (24-10-2019)

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Citer

Yirong Zhou, Yun-Long Wei, Jean Rodriguez, Yoann Coquerel. Enantioselective Organocatalytic Four-Atom Ring Expansion of Cyclobutanones: Synthesis of Benzazocinones. Angewandte Chemie International Edition, 2019, 58 (2), pp.456-460. ⟨10.1002/anie.201810184⟩. ⟨hal-02331607⟩

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