Imidazolidin-2-ones as practical, efficient chiral auxiliaries in Diels-Alder reactions
- 31 December 1992
- journal article
- research article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 3 (12) , 1553-1554
- https://doi.org/10.1016/s0957-4166(00)86059-0
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- A novel imidazolidin-2-one auxiliary for a highly stereoselective aldol route to β-hydroxyesters.Tetrahedron: Asymmetry, 1992
- Catalytic enantioselective synthesis of a key intermediate for the synthesis of prostanoidsTetrahedron Letters, 1991
- Crystalline, Enantiomerically Pure Aldols from a (‐)‐Ephedrine‐Derived N‐Acylimidazolidin‐2‐oneEuropean Journal of Inorganic Chemistry, 1991
- Synthesis of corey lactone via highly stereoselective asymmetric diels-alder reactionTetrahedron Letters, 1991
- .alpha.,.beta.-Unsaturated oxazolines, a powerful tool in asymmetric Diels-Alder cycloadditionsJournal of the American Chemical Society, 1990
- Diels-Alder reaction of dienes having stereogenic allylic substituents: control of diastereoface selectivity by the dienophileJournal of the American Chemical Society, 1988
- Asymmetric Diels-Alder cycloaddition reactions with chiral .alpha.,.beta.-unsaturated N-acyloxazolidinonesJournal of the American Chemical Society, 1988
- Synthesis of chiral isoquinuclidines and determination of their absolute configurationTetrahedron Letters, 1988
- THE CONFORMATION OF THE EPHEDRINESThe Journal of Organic Chemistry, 1950