Highly diastereoselective reduction of (−) menthylphenylglyoxalate and (−) menthylpyruvate using new hindered lithiumtrialkoxyaluminohydrides
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference10 articles.
1. Hauts rendements optiques obtenus dans la synthese d′α-alkylα-hydroxyesters par reaction d'alkoxytrialkylaluminates encombres avec le phenylglyoxalate de menthyle.
2. Synthese D'α-hydroxyacides optiquement actifs par addition d'organozinciques sur le phenylglyoxalate de (−) menthyle
3. Untersuchungen �ber asymmetrische Synthesen V. �ber den sterischen Verlauf der Reduktion von ?-Ketos�ure-estern optisch aktiver Alkohole mit Lithiumaluminiumhydrid
4. Enantiomeric purity of phenylethylene glycol and reliability of phenylglyoxylate asymmetric reductions in configurational assignments
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1. Lithium Tri-sec-butylborohydride;Encyclopedia of Reagents for Organic Synthesis;2012-03-15
2. Asymmetric reduction of β-ketoesters and chiral β-iminoesters: Impact of a α-quaternary stereocenter;Chirality;2010-10-13
3. ChemInform Abstract: Highly Diastereoselective Reduction of (-) Menthylphenylglyoxalate and (-) Menthylpyruvate Using New Hindered Lithiumtrialkoxyaluminohydrides.;ChemInform;2010-08-22
4. Lithium Tri-tert-butoxyaluminum Hydride;Encyclopedia of Reagents for Organic Synthesis;2007-09-17
5. Enantioselective Hydrogenation of α-Aryloxy α,β-Unsaturated Acids. Asymmetric Synthesis of α-Aryloxycarboxylic Acids;Organic Letters;2004-08-06
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