Nucleophilic Benzoylation Using a Mandelic Acid Dioxolanone as a Synthetic Equivalent of the Benzoyl Carbanion. Oxidative Decarboxylation of α-Hydroxyacids
Author:
Publisher
MDPI AG
Subject
Chemistry (miscellaneous),Analytical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Molecular Medicine,Drug Discovery,Pharmaceutical Science
Link
http://www.mdpi.com/1420-3049/9/5/365/pdf
Reference12 articles.
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3. Synthesis of 17-(isocyanotosylmethylene) steroids: Precursors to pregnane derivatives
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5. Phenylthiomethyllithium and Bis(phenylthio)methyllithium
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1. An efficient synthetic approach towards fully functionalized tetronic acids: the use of 1,3-dioxolane-2,4-diones as novel protected-activated synthons of α-hydroxy acids;Tetrahedron;2015-11
2. The Chemistry of α,β-Ditosyloxyketones: Novel Routes for the Synthesis of Desoxybenzoins and α-Aryl-β-ketoaldehyde Dimethylacetals from α,β-Chalcone Ditosylates;Synlett;2007-07-20
3. Chiral bis(amino alcohol)oxalamides as ligands for asymmetric catalysis. Ti(IV) catalyzed enantioselective addition of diethylzinc to aldehydes;Tetrahedron: Asymmetry;2005-03
4. Novel 2-pyrone synthesis via Michael addition of mandelic acid enolate to trans-1,2-diaroylethenes;Tetrahedron Letters;2004-11
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