Enantiomerically pure 3-p-tolylsulfinyl acrolein and crotonaldehyde dimethylacetals. Stereoselective reduction of β-keto-γ,γ-dialkoxysulfoxides
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference33 articles.
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4. Asymmetric Diels-Alder reactions of enantiopure 1-methoxy-3-(phenyl-2-hydroxyethylsulfinyl)-1,3-butadienes
5. Benzyl Methyl (S)-2-(p-Tolylsulfinyl)maleate, an Efficient Dienophile in Asymmetric Diels-Alder Reactions
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1. One-pot synthesis of α-ketoacetals from aryl methyl ketones in the presence of selenous acid catalyzed by boron trifluoride etherate;Tetrahedron Letters;2015-07
2. Efficient Preparation of α-Ketoacetals;Molecules;2012-11-22
3. Stereochemically Controlled Asymmetric 1,2-Reduction of Enones Mediated by a Chiral Sulfoxide Moiety and a Lanthanum(III) Ion;The Journal of Organic Chemistry;2011-04-28
4. ChemInform Abstract: Enantiomerically Pure 3-p-Tolylsulfinyl Acrolein and Crotonaldehyde Dimethylacetals. Stereoselective Reduction of β-Keto-γ,. gamma.-dialkoxysulfoxides.;ChemInform;2010-08-12
5. p-Tolylsulfinylmethyllithium;Encyclopedia of Reagents for Organic Synthesis;2008-09-15
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