Abstract
Tetraarylresorcinarenes in a chair conformation of C2h symmetry were synthesized by sterically oriented condensation of aromatic aldehydes with resorcinol and 2-methylresorcinol. By further phosphorylation of resorcinarenes with phosphorous amides perphosphorylated derivatives were obtained with rctt configuration of substituents at internuclear methylidene bridges. Structure of these compounds was proved using NMR spectroscopy and X-ray diffraction analysis.
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Original Russian Text © V. I. Maslennikova, O. S. Serkova, T. V. Guzeeva, L. K. Vasyanina, K. A. Lysenko, V.V. Kopteva, E. E. Nifant’ev, 2008, published in Zhurnal Obshchei Khimii, 2008, Vol. 78, No. 3, pp. 408–416.
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Maslennikova, V.I., Serkova, O.S., Guzeeva, T.V. et al. Sterically oriented synthesis and structure of new perphosphorylated resorcinarenes. Russ J Gen Chem 78, 392–401 (2008). https://doi.org/10.1134/S1070363208030092
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DOI: https://doi.org/10.1134/S1070363208030092