Intramolecular diels-alder reactions utilizing aldehyde and ketone dienophiles, a rare cycloaddition reaction

James T. Corcoran, Patrick Carberry, Dennis R. Viernes, John D. Chisholm

Research output: Contribution to journalArticle

1 Scopus citations

Abstract

Intramolecular Diels-Alder reactions have become commonly employed transformations in the repertoire of the synthetic organic chemist. Variants of this reaction, which incorporate heteroatoms in the diene and dienophile, are also popular. Surprisingly, one of the least utilized intramolecular Diels-Alder cycloadditions utilizes a carbonyl (either an aldehyde or ketone) as a dienophile. While aldehyde dienophiles are routinely used in intermolecular Diels-Alder reactions, the intramolecular variant is significantly rarer. In this mini-review we will examine the known examples of intramolecular Diels-Alder reactions utilizing aldehyde or ketone dienophiles and evaluate the advantages and challenges associated with these reactions.

Original languageEnglish (US)
Pages (from-to)149-161
Number of pages13
JournalMini-Reviews in Organic Chemistry
Volume12
Issue number2
DOIs
StatePublished - Jan 1 2015

Keywords

  • 1,3-diene
  • Aldehyde
  • Cycloaddition
  • Diels-alder
  • Ketone
  • Pyran

ASJC Scopus subject areas

  • Organic Chemistry

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