Abstract

The reaction of O-alkylated p-aminocalix[ n]arenes ( n=4, 6, 8) with N, N′-di( tert-butoxycarbonyl)thiourea in the presence of HgCl 2 and subsequent removal of the protective groups with hydrochloric acid led to the new water soluble calix[ n]guanidinium derivatives ( p-guanidiniumcalix[ n]arenes) 20– 23 . With the exception of tetraoctyl- p-guanidiniumcalix[4]arene 21 , which forms a macroscopic gelatinous aggregate even at very low concentration, all the synthesised guanidinium calixarenes show good solubility in water and sharp NMR signals. Moreover, these compounds are not cytotoxic and bind to plasmid DNA.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.