Enantioselective reduction of ketones with optically active 2,2′-diamino-6,6′-dimethylbiphenyl-lithium aluminum hydride complex
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference20 articles.
1. Asymmetric reduction with chiral reagents from lithium aluminum hydride and (S)-(-)-N-(o-substituted benzyl)-.alpha.-phenylethylamines
2. Asymmetric Reduction of Prochiral Ketones with Chiral Hydride Reagents Prepared from Lithium Aluminium Hydride and (S)-2-(N-Substituted aminomethyl)pyrrolidines
3. ENANTIOSELECTIVE REDUCTION OF KETONES WITH (+)-(1R,4S)-3-EXO-ANILINO-2-EXO-HYDROXYBORNANE-LITHIUM ALUMINIUM HYDRIDE COMPLEX
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1. Steric Modulation of Chiral Biaryl Diamines via Pd-Catalyzed Directed C−H Arylation;The Journal of Organic Chemistry;2009-02-16
2. Enantioselective reductions by chirally modified alumino- and borohydrides;Tetrahedron: Asymmetry;2001-09
3. Resolution of Enantiomers of Chiral Drugs;Methods and Principles in Medicinal Chemistry;2000-01-28
4. An efficient access to (R)- and (S)-6,6′-dimethoxy-2,2′-diiodo-1,1′-biphenyl;Tetrahedron Letters;1996-07
5. Reduction of CX to CHXH by Chirally Modified Hydride Reagents;Comprehensive Organic Synthesis;1991
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