Efficient synthesis of tetrasubstituted furans from nitroallylic acetates and 1,3-dicarbonyl/α-activating ketones by Feist-Bénary addition-elimination

Wan Yun Huang, Yi Chieh Chen, Kwunmin Chen

Research output: Contribution to journalArticle

61 Citations (Scopus)

Abstract

Pure organic: The synthesis of tetrasubstituted furans often involves transition-metal catalysis or metal-halogen exchange reactions. A new approach to these heterocycles employs the Feist-Bénary addition-elimination process using nitroallylic acetates and 1,3-dicarbonyls (see scheme; X=C, O).

Original languageEnglish
Pages (from-to)688-691
Number of pages4
JournalChemistry - An Asian Journal
Volume7
Issue number4
DOIs
Publication statusPublished - 2012 Apr 1

Fingerprint

Furans
Halogens
Ketones
Catalysis
Transition metals
Ion exchange
Acetates
Metals
Synthetic Chemistry Techniques

Keywords

  • addition
  • elimination
  • heterocycles
  • synthetic methods

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry

Cite this

Efficient synthesis of tetrasubstituted furans from nitroallylic acetates and 1,3-dicarbonyl/α-activating ketones by Feist-Bénary addition-elimination. / Huang, Wan Yun; Chen, Yi Chieh; Chen, Kwunmin.

In: Chemistry - An Asian Journal, Vol. 7, No. 4, 01.04.2012, p. 688-691.

Research output: Contribution to journalArticle

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