A new approach to remote asymmetric induction in the diastereoselective reduction of γ-keto esters by use of a chiral podand as chiral auxiliary
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Molecular Medicine
Link
http://pubs.rsc.org/en/content/articlepdf/1991/C3/C39910000799
Reference8 articles.
1. Asymmetric induction. Reduction, nucleophilic addition to, and ene reactions of chiral α-ketoesters
2. Diastereoselective Reduction of α-Keto Amides Havingtrans-2,5-Disubstituted Pyrrolidine as a Chiral Auxiliary
3. Enantioselective construction of dialkylcarbinols: synthesis of (-)-5-hexadecanolide
4. Enantioselective synthesis of 4-substituted γ-lactones
5. A Practical Method for Resolution of the Optical Isomers of 2,2′-Dihydroxy-1,1′-binaphthalene
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1. 3.15 Non-Chiral Pool Derived Synthetic Auxiliaries: Use of C2-Symmetric Chiral Diols;Comprehensive Chirality;2012
2. ChemInform Abstract: A New Approach to Remote Asymmetric Induction in the Stereoselective Reduction of γ-Keto Esters by Use of a Chiral Podand as Chiral Auxiliary.;ChemInform;2010-08-22
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4. Cascade enantioselective synthesis of γ-aryl-γ-butyrolactones with a delayed stereoselective step;Tetrahedron;2008-03
5. Update 1 of: BINOL: A Versatile Chiral Reagent;Chemical Reviews;2007-09-01
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