4.7 Article

One-pot asymmetric cyclocarbohydroxylation sequence for the enantioselective synthesis of functionalised cyclopentanes

Journal

CHEMICAL COMMUNICATIONS
Volume 46, Issue 38, Pages 7247-7249

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c0cc01940b

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Funding

  1. Universite Paul Cezanne
  2. CNRS (iSm2-UMR 6263)
  3. Ministere de l'Enseignement Superieur et de la Recherche

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A new method has been developed for the enantioselective synthesis of highly functionalised cyclopentanes bearing up to three stereogenic centres with very high stereoselectivity. This one-pot process combines an enantioselective organocatalytic Michael addition with a highly diastereoselective [3+2]-cycloaddition- fragmentation step.

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