Asymmetric Catalysis. Part 117. Novel Chiral Oxazoline Ligands for Potential Charge-Transfer Effects in the Rh(I)-Catalyzed Enantioselective Hydrosilylation. -Chiral oxazolines, such as (I) and its N-methyl derivatives (II), (III) and (IV), are synthesized in order to use them as ligands for Rh(I) c
Novel Chiral Oxazoline Ligands for Potential Charge-Transfer Effects in the Rh(I)-Catalysed Enantioselective Hydrosilylation
✍ Scribed by Henri Brunner; Reinhard Störiko; Frank Rominger
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 782 KB
- Volume
- 1998
- Category
- Article
- ISSN
- 1434-1948
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✦ Synopsis
Novel 2-(4,4'-bipyridin-2-yl)oxazolines, bearing a chiral oxazoline moiety, were synthesised starting from 4,4'bipyridine and selectively monomethylated in the N'position. After coordination to rhodium these electron-poor ligands are supposed to exhibit charge-transfer effects with electron-donating substrates in the Rh(I)-catalysed enantioselective hydrosilylation (see next publication).
📜 SIMILAR VOLUMES
Novel NЈ-methylated 2-(oxazolin-2-yl)-4,4Ј-bipyridinium salts, bearing a chiral oxazoline moiety, were tested in the Rh(I)-catalysed enantioselective hydrosilylation. After coordination to rhodium these electron-attracting ligands are supposed to exhibit charge-transfer effects with electron-donatin