Asymmetric hydride reduction using a chiral aluminium reagent modified by a crowned 2,2′-dihydroxy-1,1′-binaphthyl
- 1 January 1991
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 1
- No. 10,p. 2607-2608
- https://doi.org/10.1039/p19910002607
Abstract
The chiral aluminium hydride reagent 6 modified by a crowned 2,2′-dihydroxy-1,1′-binaphthyl 4 was found to exhibit high enantiomeric face selectivity towards a variety of prochiral carbonyl compounds including aliphatic ketones.Keywords
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