SYNTHESIS OF CHIRAL HALF-SANDWICH RHODIUM OXAZOLINE COMPLEXES AND THEIR USE AS ASYMMETRIC DIELS-ALDER CATALYSTS

Citation
Aj. Davenport et al., SYNTHESIS OF CHIRAL HALF-SANDWICH RHODIUM OXAZOLINE COMPLEXES AND THEIR USE AS ASYMMETRIC DIELS-ALDER CATALYSTS, Chemical communications, (24), 1997, pp. 2347-2348
Citations number
22
Journal title
ISSN journal
13597345
Issue
24
Year of publication
1997
Pages
2347 - 2348
Database
ISI
SICI code
1359-7345(1997):24<2347:SOCHRO>2.0.ZU;2-P
Abstract
The reaction of [(eta-C5Me5)RhCl2](2) with bidentate oxazoline contain ing ligands provides the cations [(eta-C5Me5)RhClL](+) 1-3, of which { 1, L = 2,2'-isopropylidenebis[4-isopropyl-2-oxazoline] and 3, L = 4-is opropyl-2-(2-pyridyl)-1,3-oxazoline} are structurally characterised by X-ray diffraction; treatment of these with AgSbF6 gives dications whi ch are enantioselective catalysts for the asymmetric Diels-Alder react ion between methacrolein and cyclopentadiene.