259654-57-4Relevant academic research and scientific papers
Vinylcyclopropylacyl and polyeneacyl radicals. Intramolecular ketene alkyl radical additions in ring synthesis
De Boeck, Benoit,Herbert, Nicola M. A.,Harrington-Frost, Nicole M.,Pattenden, Gerald
, p. 328 - 339 (2007/10/03)
Treatment of a variety of substituted vinylcyclopropyl selenyl esters, e.g. 11, with Bu3SnH-AIBN in refluxing benzene leads to the corresponding acyl radical intermediates, which undergo rearrangement and intramolecular cyclisations via their ketene alkyl radical equivalents producing cyclohexenones in 50-60% yield. By contrast, treatment of conjugated triene selenyl esters, e.g. 32, with Bu3SnH-AIBN produces substituted 2-cyclopentenones via intramolecular cyclisations of their ketene alkyl radical intermediates. Under the same radical-initiating conditions the selenyl esters derived from o-vinylbenzoic acid and o-vinylcinnamic acid undergo intramolecular cyclisations producing 1-indanone and 5,6-dihydrobenzocyclohepten-7-one respectively in 60-70% yields. A tandem radical cyclisation from the α,β,γ, δ-diene selenyl ester 31 provides an expeditious synthesis of the diquinane 35 in 69% yield.
Novel intramolecular cyclisations involving ketene radical intermediates as an approach to the synthesis of polyquinanes
Harrington-Frost, Nicole M.,Pattenden, Gerald
, p. 1917 - 1918 (2007/10/03)
Treatment of the polyene selenyl ester 1 with Bu3SnH-AIBN leads to a concise synthesis of the diquinane 6 via a novel cyclisation involving a ketenyl radical intermediate. By contrast under the same radical initiating conditions the selenyl est
