Literature DB >> 16872217

Highly stereoselective oxidative esterification of aldehydes with beta-dicarbonyl compounds.

Woo-Jin Yoo1, Chao-Jun Li.   

Abstract

Copper-catalyzed oxidative esterification of aldehydes with beta-dicarbonyl compounds was developed using tert-butyl hydroperoxide as an oxidant. In general, the enol esters were synthesized in good yields (up to 87%) and high stereoselectivity under the optimized reaction conditions.

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Year:  2006        PMID： 16872217     DOI： 10.1021/jo0606103

Source DB:  PubMed          Journal:  J Org Chem        ISSN： 0022-3263            Impact factor:   4.354


  3 in total

1.  Photocatalytic C-H Activation and Oxidative Esterification Using Pd@g-C3N4.

Authors:  Sanny Verma; R B Nasir Baig; Mallikarjuna N Nadagouda; Rajender S Varma
Journal:  Catal Today       Date:  2018       Impact factor: 6.766

2.  Scope and Mechanistic Investigations on the Solvent-Controlled Regio- and Stereoselective Formation of Enol Esters from the Ruthenium-Catalyzed Coupling Reaction of Terminal Alkynes and Carboxylic Acids.

Authors:  Chae S Yi; Ruili Gao
Journal:  Organometallics       Date:  2009-10-30       Impact factor: 3.876

Review 3.  Cross-dehydrogenative coupling for the intermolecular C-O bond formation.

Authors:  Igor B Krylov; Vera A Vil'; Alexander O Terent'ev
Journal:  Beilstein J Org Chem       Date:  2015-01-20       Impact factor: 2.883
  3 in total

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