Issue 24, 1997

Synthesis of chiral half-sandwich rhodium oxazoline complexes and their use as asymmetric Diels–Alder catalysts

Abstract

The reaction of [(η-C5Me5)RhCl2]2 with bidentate oxazoline containing ligands provides the cations [(η-C5Me5)RhClL]+ 1–3, of which {1, L = 2,2′-isopropylidenebis[4-isopropyl-2-oxazoline] and 3, L = 4-isopropyl-2-(2-pyridyl)-1,3-oxazoline} are structurally characterised by X-ray diffraction; treatment of these with AgSbF6 gives dications which are enantioselective catalysts for the asymmetric Diels–Alder reaction between methacrolein and cyclopentadiene.

Article information

Article type
Paper

Chem. Commun., 1997, 2347-2348

Synthesis of chiral half-sandwich rhodium oxazoline complexes and their use as asymmetric Diels–Alder catalysts

A. J. Davenport, J. Fawcett, L. Lad and D. R. Russell, Chem. Commun., 1997, 2347 DOI: 10.1039/A706287G

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