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Trienamines: Their Key Role in Extended Organocatalysis for Diels-Alder Reactions

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Activation via trienamine intermediates is a synthetically useful protocol for performing asymmetric Diels-Alder reactions controlled by a remote chiral catalyst (a secondary or primary amine). Key features underpinning this concept are the conformation towards the trienamine formation and also the use of highly electrophilic dienophiles. This cycloaddition reaction allows the application of asymmetric organocatalysis at a remote position, and the synthesis of complex molecules short synthetic sequences is possible.

Opis fizyczny
  • Departamento de Química Orgánica I,
    Facultad de Químicas, Universidad
    Complutense de Madrid
  • Departamento de Química Orgánica
    (Módulo 1), Facultad de Ciencias,
    Universidad Autónoma de Madrid
    Cantoblanco, 28049-Madrid,
  • Departamento de Química Orgánica
    (Módulo 1), Facultad de Ciencias,
    Universidad Autónoma de Madrid
    Cantoblanco, 28049-Madrid,
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