Interplay of ortho- with spiro-cyclisation during iminyl radical closures onto arenes and heteroarenes

Roy Thomas McBurney*, John Christopher Walton*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

25 Citations (Scopus)
3 Downloads (Pure)

Abstract

Sensitised photolyses of ethoxycarbonyl oximes of aromatic and heteroaromatic ketones yielded iminyl radicals which were characterised by EPR spectrscopy. Iminyls with suitably placed arene or heteroarene acceptors underwent cyclisations yielding phenanthridine type products from ortho-additions. For benzofuran and benzothiophene acceptors, spiro-cyclisation predominated at low temperatures but thermodynamic control ensured ortho-products, benzofuro- or benzothieno-isoquinolines, formed at higher temperatures. Estimates by steady state kinetic EPR established that iminyl radical cyclisations onto aromatics took place about an order of magnitule more slowly than prototypical C-centred radicals. Cyclisation energetics were investigated by DFT computations which gave insights into factors influencing the two cyclisation modes.
Original languageEnglish
Pages (from-to)1083-1092
Number of pages10
JournalBeilstein Journal of Organic Chemistry
Volume9
DOIs
Publication statusPublished - 4 Jun 2013

Keywords

  • Cyclisation
  • EPR spectroscopy
  • Free radicals
  • Heterocycles
  • Oxime carbonates

Fingerprint

Dive into the research topics of 'Interplay of ortho- with spiro-cyclisation during iminyl radical closures onto arenes and heteroarenes'. Together they form a unique fingerprint.

Cite this