Abstract
Triaroylbenzenes connected via m-xylyl, p-xylyl, 4,4'-biphenyl, and 1,3,5-benzenetriyl linking units have been prepared in good yield by condensation of bis(enaminones) with aryl ethynyl ketones. The required bis(enaminones) were conveniently prepared starting from the corresponding bis- or tris(halomethyl) linking units and 3-hydroxybenzaldehyde. (C) 2000 Elsevier Science Ltd.
Author supplied keywords
Cite
CITATION STYLE
APA
Pigge, F. C., & Ghasedi, F. (2000). Synthesis of linked 1,3,5-triaroylbenzenes via enamine-directed alkyne cyclotrimerization. Tetrahedron Letters, 41(34), 6545–6549. https://doi.org/10.1016/S0040-4039(00)01125-4
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.
Already have an account? Sign in
Sign up for free