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Double Catalytic Kinetic Resolution (DoCKR) of Acyclic anti-1,3-Diols: The Additive Horeau Amplification.
Merad, Jérémy; Borkar, Prashant; Caijo, Frédéric; Pons, Jean-Marc; Parrain, Jean-Luc; Chuzel, Olivier; Bressy, Cyril.
Affiliation
  • Merad J; Aix Marseille Université, CNRS, Centrale Marseille, iSm2, Marseille, France.
  • Borkar P; Aix Marseille Université, CNRS, Centrale Marseille, iSm2, Marseille, France.
  • Caijo F; DemetaSAS, 6 rue Pierre Joseph Colin, Biopole, 35500, Rennes, France.
  • Pons JM; Aix Marseille Université, CNRS, Centrale Marseille, iSm2, Marseille, France.
  • Parrain JL; Aix Marseille Université, CNRS, Centrale Marseille, iSm2, Marseille, France.
  • Chuzel O; Aix Marseille Université, CNRS, Centrale Marseille, iSm2, Marseille, France.
  • Bressy C; Aix Marseille Université, CNRS, Centrale Marseille, iSm2, Marseille, France.
Angew Chem Int Ed Engl ; 56(50): 16052-16056, 2017 12 11.
Article de En | MEDLINE | ID: mdl-29024411
ABSTRACT
The concept of a synergistic double catalytic kinetic resolution (DoCKR) as described in this article was successfully applied to racemic acyclic anti-1,3-diols, a common motif in natural products. This process takes advantage of an additive Horeau amplification involving two successive enantioselective organocatalytic acylation reactions, and leads to diesters and recovered diols with high enantiopurities. It was first developed with C2 -symmetrical diols and then further extended to non-C2 -symmetrical anti diols to prepare useful chiral building blocks. The protocol is highly practical as it only requires 1 mol % of a commercially available organocatalyst and leads to easily separable products. This procedure was applied to the shortest reported total synthesis of (+)-cryptocaryalactone, a natural product with anti-germinative activity.
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Type d'étude: Guideline Langue: En Journal: Angew Chem Int Ed Engl Année: 2017 Type de document: Article Pays d'affiliation: France

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Type d'étude: Guideline Langue: En Journal: Angew Chem Int Ed Engl Année: 2017 Type de document: Article Pays d'affiliation: France