Unexpected dimerization during hydrogenation of 2-(2-pyridylmethylene)-3(2H)-benzofuran-3-ones

Marianna Mák, Mihály Nógrádi, A. Szöllösy

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

Palladium catalyzed hydrogenation of 2-(2-pyridylmethylene)-3(2H)-benzofuran-3-ones (1-3) gave besides the expected 2,α-dihydro products 8-10 pentacyclic dimers formed by an attack of a semihydrogenated species on the substrate.

Original languageEnglish
Pages (from-to)8425-8429
Number of pages5
JournalTetrahedron
Volume62
Issue number35
DOIs
Publication statusPublished - Aug 28 2006

Fingerprint

Hydrogenation
Dimerization
Palladium
Dimers
Substrates
benzofuran

Keywords

  • 2-Pyridylmethylene-3(2H)-benzofuran-3-ones
  • Dimerization
  • Hydrogenation

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Unexpected dimerization during hydrogenation of 2-(2-pyridylmethylene)-3(2H)-benzofuran-3-ones. / Mák, Marianna; Nógrádi, Mihály; Szöllösy, A.

In: Tetrahedron, Vol. 62, No. 35, 28.08.2006, p. 8425-8429.

Research output: Contribution to journalArticle

Mák, Marianna ; Nógrádi, Mihály ; Szöllösy, A. / Unexpected dimerization during hydrogenation of 2-(2-pyridylmethylene)-3(2H)-benzofuran-3-ones. In: Tetrahedron. 2006 ; Vol. 62, No. 35. pp. 8425-8429.
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