Studies on novel and chiral 1,4-dihydropyridines. III. Asymmetric reduction of some ketones with novel NADH model compounds, (SS)-3-(p-Tolylsulfinyl)-1,4-dihydropyridines
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference31 articles.
1. NADH mimics for the stereoselective reduction of benzoylformates to the corresponding mandelates.
2. Reduction by a model of NAD(P)H. Effect of metal ion and stereochemistry on the reduction of .alpha.-keto esters by 1,4-dihydronicotinamide derivatives
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2. Enantioselective Desymmetrization of 1,4‐Dihydropyridines by Oxidative NHC Catalysis;Chemistry – A European Journal;2019-05-08
3. Synthetic Methods of α-Pyridinyl and α-Bipyridinyl Alcohols and α,α'-Pyridine and α,α'-Bipyridine Diols;Current Organic Synthesis;2015-05-08
4. The coordination chemistry of organo-hydride donors: new prospects for efficient multi-electron reduction;Chemical Society Reviews;2013
5. Enantioselective Organocatalytic Aza-Ene-Type Domino Reaction Leading to 1,4-Dihydropyridines;The Journal of Organic Chemistry;2011-02-15
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