Aluminate(1-), [(1R)-[1,1′-Binaphthalene]-2,2′-diolato(2-)-κO2,κO2′]ethoxyhydro-, Lithium (1:1)
Author:
Affiliation:
1. SABIC Research & Technology Pvt Ltd; Bangalore India
Publisher
John Wiley & Sons, Ltd
Reference16 articles.
1. Virtually complete enantioface differentiation in carbonyl group reduction by a complex aluminum hydride reagent
2. Recent developments in asymmetric reduction of ketones with biocatalysts
3. First example of asymmetric transfer hydrogenation in water induced by a chiral amino alcohol hydrochloride
4. Lithium-B-Iso-2-ethylapopinocampheyl-9-borabicyclo[3.3.1]nonyl hydride as an improved reagent for asymmetric reduction of unhindered aliphatic ketones. Further evidence for the improved enantioselectivity in reductions by reagents containing increased steric requirements at the 2-position of the apopinene structure
5. Stereoselective introduction of hydroxy-groups into the 24-, 25-, and 26-positions of the cholesterol side chain
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