Asymmetric Reduction with C1- and C2-Symmetric NADH Model Compounds Containing Chiral 1,1′-Binaphthyls
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/56/12/56_12_3672/_pdf
Reference21 articles.
1. Asymmetric induction. 2. Enantioselective alkylation of cyclohexanone via a chiral enamine
2. Virtually complete enantioface differentiation in carbonyl group reduction by a complex aluminum hydride reagent
3. High enantioselectivity in reductions with a chiral bis(NADH) model compound
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2. Synthesis of orthogonally protected biaryl amino acid derivatives;Organic & Biomolecular Chemistry;2006
3. Non-Symmetrically Substituted 1,1‘-Binaphthyls in Enantioselective Catalysis;Chemical Reviews;2003-07-29
4. The first example of enantioselective isocyanosilylation of meso epoxides with TMSCN catalyzed by novel chiral organogallium and indium complexesElectronic supplementary information (ESI) available: Characterization data, chiral analysis and determination of absolute configuration. See http://www.rsc.org/suppdata/cc/b2/b212511k/;Chemical Communications;2003-02-13
5. Synthesis and highly ordered thin films of optically active 2′-methoxy-1,1′-binaphthyl substituted phthalocyanines;Synthetic Metals;2002-11
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