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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).


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ChemInform Abstract: Asymmetric Catalysi
✍ H. BRUNNER; R. STOERIKO; F. ROMINGER 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 1 views

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

Rh(I)-Catalysed Asymmetric Hydrosilylati
✍ Henri Brunner; Reinhard Störiko 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 521 KB

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