CHIRAL HYDRIDE REAGENTS CONTAINING (R/S)-2,2′-DIHYDROXY-6,6′-DIMETHYLBIPHENYL FOR REDUCTION OF ALKYL PHENYL KETONES
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
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1. Virtually complete enantioface differentiation in carbonyl group reduction by a complex aluminum hydride reagent
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3. Asymmetric Reduction of Aromatic Ketones with Reagents Prepared from NaBH4and ZnCl2in the Presence of 1,2 : 5,6-Di-O-isopropylidene-α-D-glucofuranose
4. Enantioselective reduction of ketones with optically active 2,2′-diamino-6,6′-dimethylbiphenyl-lithium aluminum hydride complex
5. Asymmetric reduction of aromatic ketones with borane-amine complexes modified with optically pure 2,2′-dihydroxy-6,6′-dimethylbiphenyl
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1. C2 and C1 Symmetry of chiral auxiliaries in catalytic reactions on metal complexes;Tetrahedron;2008-02
2. Chiral oxazoline route to enantiomerically pure biphenyls: magnesio and copper mediated asymmetric hetero- and homo-coupling reactions;Tetrahedron;2004-05
3. Enantioselective reductions by chirally modified alumino- and borohydrides;Tetrahedron: Asymmetry;2001-09
4. Preparation of New Binaphthol-Based Tridentate Ligands for Enantioselective Synthesis;Collection of Czechoslovak Chemical Communications;2000
5. An asymmetric synthesis of a C2 symmetric tetrasubstituted biaryl: 2,2′-Dihydroxy-6,6′-dimethyl-1,1′-biphenyl, a stable chiral system;Tetrahedron Letters;1993-10
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