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Delany, E. G. ; Fagan, C.-L. ; Gundala, S. ; Mari, A. ; Broja, Thomas ; Zeitler, Kirsten ; Connon, S. J.

NHC-catalysed aerobic aldehyde-esterifications with alcohols: no additives or cocatalysts required

Delany, E. G., Fagan, C.-L., Gundala, S. , Mari, A., Broja, Thomas, Zeitler, Kirsten and Connon, S. J. (2013) NHC-catalysed aerobic aldehyde-esterifications with alcohols: no additives or cocatalysts required. Chemical Communications 49, pp. 6510-6512.

Date of publication of this fulltext: 03 Aug 2016 10:53
Article
DOI to cite this document: 10.5283/epub.34220


Abstract

A highly efficient, broad scope, additive-free mild protocol for the oxidative carbene-catalysed esterification of aldehydes (including the related aqueous oxidation to acids) has been developed.



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Details

Item typeArticle
Journal or Publication TitleChemical Communications
Publisher:ROYAL SOC CHEMISTRY
Place of Publication:CAMBRIDGE
Volume:49
Page Range:pp. 6510-6512
Date2013
InstitutionsChemistry and Pharmacy > Institut für Organische Chemie > Alumni or Retired Professors > Arbeitskreis Dr. Kirsten Zeitler
Identification Number
ValueType
10.1039/c3cc42596gDOI
KeywordsHETEROCYCLIC CARBENE CATALYSIS; ALPHA-KETO ACIDS; AROMATIC-ALDEHYDES; OXIDATIVE ESTERIFICATION; CATIONIC MICELLE; THIAZOLIUM IONS; STEREOSELECTIVE-SYNTHESIS; FACILE OXIDATION; ACTIVE ALDEHYDES; REDOX ACTIVATION;
Dewey Decimal Classification500 Science > 540 Chemistry & allied sciences
StatusPublished
RefereedYes, this version has been refereed
Created at the University of RegensburgYes
URN of the UB Regensburgurn:nbn:de:bvb:355-epub-342205
Item ID34220

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