Halogenation effects in intramolecular furan Diels-Alder reactions: Broad scope synthetic and computational studies

Robert L. Rae, Justyna M. Zurek, Martin J. Paterson, Magnus Bebbington

Research output: Contribution to journalArticle

9 Citations (Scopus)

Abstract

For the first time a comprehensive synthetic and computational study of the effect of halogen substitution on both furan and dienophile for the intramolecular Furan Diels-Alder (IMDAF) reaction has been undertaken. Contrary to our initial expectations, halogen substitution on the dienophile was found to have a significant effect, making the reactions slower and less thermodynamically favourable. However, careful choice of the site of furan halogenation could be used to overcome dienophile halogen substitution, leading to highly functionalised cycloadducts. These reactions are thought to be controlled by the interplay of three factors: positive charge stabilisation in the transition state and product, steric effects and a dipolar interaction term identified by high level calculations. Frontier orbital effects do not appear to make a major contribution in determining the viability of these reactions, which is consistent with our analysis of calculated transition state structural data.

Original languageEnglish
Pages (from-to)7946-7952
Number of pages7
JournalOrganic and Biomolecular Chemistry
Volume11
Issue number45
DOIs
StatePublished - 7 Dec 2013

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Halogenation
halogenation
Diels-Alder reactions
Halogens
furans
Cycloaddition Reaction
Substitution reactions
halogens
substitutes
Stabilization
viability
stabilization
orbitals
furan
products
interactions

Cite this

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Halogenation effects in intramolecular furan Diels-Alder reactions : Broad scope synthetic and computational studies. / Rae, Robert L.; Zurek, Justyna M.; Paterson, Martin J.; Bebbington, Magnus.

In: Organic and Biomolecular Chemistry, Vol. 11, No. 45, 07.12.2013, p. 7946-7952.

Research output: Contribution to journalArticle

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AU - Paterson, Martin J.

AU - Bebbington, Magnus

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