Preparation of heterocycles by microwave-induced retro Diels-Alder reaction

Ferenc Miklós, G. Stájer, F. Fülöp

Research output: Contribution to journalArticle

11 Citations (Scopus)

Abstract

Pyrimidinone, thioxopyrimidinone, pyrimido[2,1-a]phthalazinone and [1,3]oxazino[2,3-a] isoindolone were obtained by means of microwave-assisted [4+2] cycloreversion. The microwave heating of the parent norbornene or oxanorbornene fused compounds in a solvent with a medium or large loss factor generates retro Diels-Alder products in excellent yield and high purity.

Original languageEnglish
Pages (from-to)915-916
Number of pages2
JournalLetters in Organic Chemistry
Volume3
Issue number12
DOIs
Publication statusPublished - Dec 2006

Fingerprint

Pyrimidinones
Microwave heating
Cycloaddition Reaction
Microwaves
Heating
2-norbornene
Isoindol-1-one

Keywords

  • Microwave
  • N
  • N- and O
  • N-heterocycles
  • Retro Diels-Alder reaction

ASJC Scopus subject areas

  • Organic Chemistry
  • Biochemistry

Cite this

Preparation of heterocycles by microwave-induced retro Diels-Alder reaction. / Miklós, Ferenc; Stájer, G.; Fülöp, F.

In: Letters in Organic Chemistry, Vol. 3, No. 12, 12.2006, p. 915-916.

Research output: Contribution to journalArticle

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