A [2+2+2]-Cyclotrimerization Approach to Selectively Substituted Fluorenes and Fluorenols, and Their Conversion to 9,9'-Spirobifluorenes
Status PubMed-not-MEDLINE Language English Country Germany Media print-electronic
Document type Journal Article
- Keywords
- aromatic compounds, catalysis, cycloaddition, rhodium, spiro compounds,
- Publication type
- Journal Article MeSH
Synthesis of selectively substituted fluorenes and fluorenols was achieved by using catalytic [2+2+2]cyclotrimerization. Various starting diynes were reacted with different alkynes in the presence of a catalytic amount of Wilkinson's catalyst (RhCl(PPh3)3) providing the compounds possessing the fluorene scaffold in good isolated yields. A set of four regioselectively substituted fluorenols was converted to the corresponding 9,9'-spirobifluorenes and their spectral characteristics were measured.
References provided by Crossref.org
Cyclotrimerization Approach to Symmetric [9]Helical Indenofluorenes: Diverting Cyclization Pathways