Asymmetric grignard cross-coupling by means of polymer-supported optically active β-dimethylaminoalkylphosphine-nickel catalysts
- 31 December 1980
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 21 (48) , 4623-4626
- https://doi.org/10.1016/0040-4039(80)80090-6
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Chiral β-dimethylaminoalkylphosphines. Highly efficient ligands for a nickel complex catalyzed asymmetric grignard cross-coupling reactionTetrahedron Letters, 1980
- Transition-metal-catalyzed asymmetric organic synthesis via polymer-attached optically active phosphine ligands. 4. Asymmetric hydroformylationThe Journal of Organic Chemistry, 1979
- CATALYTIC ASYMMETRIC HYDROGENATIONS WITH POLYMER SUPPORTED CHIRAL PYRROLIDINEPHOSPHINE–RHODIUM COMPLEXESChemistry Letters, 1978
- Transition metal catalyzed asymmetric organic syntheses via polymer-attached optically active phosphine ligands. Synthesis of R amino acids by hydrogenation with a polymer catalyst containing optically active alcohol sitesJournal of the American Chemical Society, 1978
- Transition metal catalyzed asymmetric organic syntheses via polymer-attached optically active phosphine ligands. Synthesis of R amino acids and hydratropic acid by hydrogenationJournal of the American Chemical Society, 1978
- High stereoselectivity in asymmetric Grignard cross-coupling catalyzed by nickel complexes of chiral (aminoalkylferrocenyl)phosphinesJournal of the American Chemical Society, 1976
- Selective hydrogenation of ketones and olefins over polymer-bound rhodium catalystsInorganica Chimica Acta, 1975
- Asymmetric catalytic reduction with transition metal complexes. II. Asymmetric catalysis by a supported chiral rhodium complexJournal of the American Chemical Society, 1973