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Highly Enantioselective Copper-Catalyzed Conjugate Addition of Diethylzinc to Enones Using Chiral Spiro Phosphoramidites as Ligands.
- Source :
-
Journal of Organic Chemistry . 2/21/2003, Vol. 68 Issue 4, p1582. 3p. 2 Diagrams, 3 Charts. - Publication Year :
- 2003
-
Abstract
- Novel monodentate chiral spiro phosphoramidite ligands have been readily synthesized in good yields from enantiomerically pure 1,1'-spirobiindane-7,7'-diol. The new ligands were highly efficient in the copper-catalyzed conjugate addition of Et[sub 2]Zn to enones with up to 98% enantiomeric excess. [ABSTRACT FROM AUTHOR]
- Subjects :
- *LIGANDS (Chemistry)
*CHIRAL drugs
*CARBONYL compounds
Subjects
Details
- Language :
- English
- ISSN :
- 00223263
- Volume :
- 68
- Issue :
- 4
- Database :
- Academic Search Index
- Journal :
- Journal of Organic Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 9198280
- Full Text :
- https://doi.org/10.1021/jo026611m