Asymmetric synthesis of tertiary vinyl carbinols by highly stereoselective methylation of α-methyl-β-ketosulfoxides with aluminum reagents
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference53 articles.
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2. Alkylation of enones and ketones using substituted alkyl- and arylaluminum compounds
3. Alkylaluminum halides
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5. Stereoselective addition of organoaluminium or organomanganese reagents to 2-methyl-3—oxo amides (or esters) providing erythro or threo 2-methyl-3-hydroxy amides (or esters)
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1. Remote induction of stereoselective 1,2-addition of aryl Grignard reagents to β-sulfinyl enones;Tetrahedron Letters;2014-01
2. 1.03 Organoaluminum Reagents;Comprehensive Organic Synthesis II;2014
3. Vinyl sulfone- and vinyl sulfoxide-modified tetrahydrofurans: a preliminary account of the enantiomeric synthesis of and diastereoselectivity of addition to new classes of Michael acceptors;Tetrahedron;2013-10
4. Switchable Palladium-Catalyst Reaction of Bromomethyl Sulfoxides, CO, and N-Nucleophiles: Aminocarbonylation at Csp3 versus Oxidative Carbonylation of Amines;The Journal of Organic Chemistry;2012-10-16
5. 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
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