4.5 Article

Ruthenium-Catalyzed [2+2+2] Bis-Homo-Diels-Alder Cycloadditions of 1,5-Cyclooctadiene with Alkynyl Phosphonates

Journal

SYNTHESIS-STUTTGART
Volume 51, Issue 22, Pages 4271-4278

Publisher

GEORG THIEME VERLAG KG
DOI: 10.1055/s-0039-1690612

Keywords

1,5-cyclooctadiene; bis-homo-Diels-Alder reaction; cyclo-addition; ruthenium-catalyzed; alkynyl phosphonate

Funding

  1. Natural Sciences and Engineering Council of Canada (NSERC)

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The ruthenium-catalyzed [2+2+2] bis-homo-Diels-Alder cycloaddition between 1,5-cyclooctadiene and alkynyl phosphonates was investigated. Various alkynyl phosphonate moieties were found to be compatible with the cycloaddition to give the tricyclo[4.2.2.0(2,5)]dec-7-enetricyclic compounds in yields of 46-97%.

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