Synthesis of calix[4]resorcinarenes,containing phosphoryl fragments at the lower rim of the molecule |
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Authors: | A R Burilov I R Knyazeva Yu M Sadykova M A Pudovik W D Habicher I Baier A I Konovalov |
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Institution: | (1) A. E. Arbuzov Institute of Organic and Physical Chemistry, Kazan Research Center of the Russian Academy of Sciences, 8 ul. Akad. Arbuzova, 420088 Kazan, Russian Federation;(2) Institute of Organic Chemistry, Dresden University of Technology, 13 Mommsenstrasse, D-01062 Dresden, Germany |
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Abstract: | Reaction of resorcinol with phosphorylated acetals or ethoxyvinylphosphonic acid esters in acidic media leads to calix4]resorcinarenes,
containing dialkoxyphosphoryl fragments at the lower rim of the molecule. When the alkyl substituent in alkoxy groups at phosphorus
atom is not very long, a partial hydrolysis of the initially formed products takes place to give calixarenes with alkoxyhydroxyphosphoryl
fragments.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 6, pp. 1102–1106, June, 2007. |
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Keywords: | acetals vinylphosphonic acids resorcinols calix[4]resorcinarenes organophosphorus compounds |
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