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Article
Selective pyrone functionalization: reductive alkylation of triacetic acid lactone
Tetrahedron Letters
  • George A. Kraus, Iowa State University
  • Kevin Basemann, Iowa State University
  • Tezcan Guney, Iowa State University
Document Type
Article
Disciplines
Publication Version
Accepted Manuscript
Publication Date
12-1-2014
DOI
10.1016/j.tetlet.2015.01.141
Abstract

The one-pot reaction of aldehydes, triacetic acid lactone, and Hantzsch 1,4-dihydropyridine affords 3-alkyl pyrones via a reductive alkylation strategy.

Comments

This is a manuscript of an article published as Kraus, George A., Kevin Basemann, and Tezcan Guney. "Selective pyrone functionalization: reductive alkylation of triacetic acid lactone." Tetrahedron Letters 56, no. 23 (2015): 3494-3496. 10.1016/j.tetlet.2015.01.141. Posted with permission.

Creative Commons License
Creative Commons Attribution-NonCommercial-No Derivative Works 4.0 International
Copyright Owner
Elsevier Ltd.
Language
en
File Format
application/pdf
Citation Information
George A. Kraus, Kevin Basemann and Tezcan Guney. "Selective pyrone functionalization: reductive alkylation of triacetic acid lactone" Tetrahedron Letters Vol. 56 Iss. 3 (2014) p. 3494 - 3496
Available at: http://works.bepress.com/george_kraus/227/