A Comparison of Macrocyclization Strategies for the Selective Synthesis of [8], [10], [12], [15], and
Taiwo S Adepoju1, Jacob K Istre1, Bradley L Merner1
1Department of Chemistry and Biochemistry, Auburn University, Auburn, Alabama 36830, United States.
Abstract:
The size-selective synthesis of [8], [10], [12], [15], and [16]cycloparaphenylene (CPP) is reported. The syntheses compare Suzuki-Miyaura and Pt-square-based macrocyclization strategies and feature a dehydrative aromatization reaction of macrocyclic cyclohex-2-ene-1,4-diols to furnish the carbon nanohoops. These unsaturated diols have proven to be versatile arene surrogates, enabling the synthesis of highly strained p-terphenyl-containing macrocycles, as well as functionalized and substituted bent p-phenylene units. This report represents the first time this aromatization protocol has been employed in the synthesis of [n]CPPs.
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