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The reaction of octa-2-hydroxyethylated calix[4]resorcinols with phosphorous acid amides and the subsequent thionylation by elemental sulfur afforded hydrolytically stable oxyethyl calix[4]resorcinols containing eight thiophosphoryl fragments. Click to show full abstract
The reaction of octa-2-hydroxyethylated calix[4]resorcinols with phosphorous acid amides and the subsequent thionylation by elemental sulfur afforded hydrolytically stable oxyethyl calix[4]resorcinols containing eight thiophosphoryl fragments.
Keywords:
acid amides;
resorcinols phosphorous;
calix resorcinols;
phosphorous acid;
calix;
phosphorylation oxyethylated
Journal Title: Russian Journal of General Chemistry
Year Published: 2018
Link to full text (if available)
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Journal Title: Russian Journal of General Chemistry
Year Published: 2018
Link to full text (if available)
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recommendations!