Preparation of bicyclo[4.3.0]nonanes by an organocatalytic intramolecular Diels-Alder reaction

European Journal of Organic Chemistry

Volumn , Issue 8, 2005, Pages 1620-1624

  Selkälä, Sami A ^a   Koskinen, Ari M P ^a  

^a AALTO UNIVERSITY   (Finland)

Author keywords

Cycloaddition; Enantioselectivity; Natural products; Organocatalysis

Indexed keywords

EID: 18144394744     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/ejoc.200400802     Document Type: Article

References (51)

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51. The opposite enantiomer has been synthesized by use of the pure (R) enantiomer of phenyloxazolidinone as a covalently attached chiral auxiliary. Its structure and absolute and relative stereochemistry were determined by X-ray crystallography: S. A. Selkälä, Ph.D. Thesis (Total synthesis of amaminol A), 2003, Helsinki University of Technology.