Highly diastereoselective Michael reaction under solvent-free conditions using microwaves: Conjugate addition of flavanone to its chalcone precursor

T. Patonay, Rajender S. Varma, András Vass, A. Lévai, József Dudás

Research output: Contribution to journalArticle

45 Citations (Scopus)

Abstract

Microwave-assisted reaction of 2′-hydroxychalcones in the presence of DBU resulted in the formation of hitherto unknown dimers by conjugate addition of the intermediate cyclic ketone to the starting enone.

Original languageEnglish
Pages (from-to)1403-1406
Number of pages4
JournalTetrahedron Letters
Volume42
Issue number8
DOIs
Publication statusPublished - Feb 19 2001

Fingerprint

Chalcone
Microwaves
Ketones
Dimers
flavanone
2'-hydroxychalcone

Keywords

  • Addition reactions
  • Chalcones
  • Dimers
  • Flavanones
  • Microwave heating

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Highly diastereoselective Michael reaction under solvent-free conditions using microwaves : Conjugate addition of flavanone to its chalcone precursor. / Patonay, T.; Varma, Rajender S.; Vass, András; Lévai, A.; Dudás, József.

In: Tetrahedron Letters, Vol. 42, No. 8, 19.02.2001, p. 1403-1406.

Research output: Contribution to journalArticle

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AU - Lévai, A.

AU - Dudás, József

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