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3 results on '"tetraoxadithiacalix[6]arene"'

1. Synthesis of Polyfluorinated Thia- and Oxathiacalixarenes Based on Perfluoro-m-xylene

Author

Vladimir N. Kovtonyuk, Yuri V. Gatilov, Pavel V. Nikul’shin, and Roman A. Bredikhin

Subjects
perfluorinated tetrathiacalix[4]arene, perfluoro-m-xylene, dioxadithiacalix[4]arenes, tetraoxadithiacalix[6]arene, thiourea, 2,5-difluoro-4,6-bis(trifluoromethyl)benzene-1,3-dithiol, Organic chemistry, QD241-441
Abstract

Perfluorinated tetrathiacalix[4]arene was obtained by heating perfluoro-m-xylene with thiourea or 2,5-difluoro-4,6-bis(trifluoromethyl)benzene-1,3-dithiol at 90 °C. Interaction of perfluoro-m-xylene with resorcinol or orcinol under mild conditions and subsequent heating of the mixture with 2,5-difluoro-4,6-bis(trifluoromethyl)benzene-1,3-dithiol leads to polyfluorinated dioxadithiacalix[4]arenes. Triphenyl and pentaphenyl ethers formed by the interaction of perfluoro-m-xylene with resorcinol under heating with thiourea gives polyfluorinated oxathiacalixarenes containing six and five aromatic nuclei, respectively.

Published
2021
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2. Synthesis of Polyfluorinated Thia- and Oxathiacalixarenes Based on Perfluoro-m-xylene

Author

Yuri V. Gatilov, Roman A. Bredikhin, Pavel V. Nikul’shin, and Vladimir N. Kovtonyuk

Subjects
tetraoxadithiacalix[6]arene, Pharmaceutical Science, Resorcinol, Sulfides, Xylenes, Orcinol, Medicinal chemistry, Article, Analytical Chemistry, lcsh:QD241-441, perfluoro-m-xylene, chemistry.chemical_compound, lcsh:Organic chemistry, Phenols, dioxadithiacalix[4]arenes, Drug Discovery, Benzene Derivatives, Physical and Theoretical Chemistry, thiourea, Fluorocarbons, Trifluoromethyl, X-ray analyses, perfluorinated tetrathiacalix[4]arene, Organic Chemistry, Benzene, m-Xylene, Biodegradation, Environmental, chemistry, Thiourea, Chemistry (miscellaneous), Molecular Medicine, 2,5-difluoro-4,6-bis(trifluoromethyl)benzene-1,3-dithiol, Calixarenes, Toluene
Abstract

Perfluorinated tetrathiacalix[4]arene was obtained by heating perfluoro-m-xylene with thiourea or 2,5-difluoro-4,6-bis(trifluoromethyl)benzene-1,3-dithiol at 90 &deg, C. Interaction of perfluoro-m-xylene with resorcinol or orcinol under mild conditions and subsequent heating of the mixture with 2,5-difluoro-4,6-bis(trifluoromethyl)benzene-1,3-dithiol leads to polyfluorinated dioxadithiacalix[4]arenes. Triphenyl and pentaphenyl ethers formed by the interaction of perfluoro-m-xylene with resorcinol under heating with thiourea gives polyfluorinated oxathiacalixarenes containing six and five aromatic nuclei, respectively.

Published
2021

3. Synthesis of Polyfluorinated Thia- and Oxathiacalixarenes Based on Perfluoro- m -xylene.

Author

Kovtonyuk, Vladimir N., Gatilov, Yuri V., Nikul'shin, Pavel V., Bredikhin, Roman A., Curtis, Anthony D.M., Cragg, Peter, and Matthews, Susan E.

Subjects
*RESORCINOL, *THIOUREA, *AROMATIC compounds, *ETHERS
Abstract

Perfluorinated tetrathiacalix[4]arene was obtained by heating perfluoro-m-xylene with thiourea or 2,5-difluoro-4,6-bis(trifluoromethyl)benzene-1,3-dithiol at 90 °C. Interaction of perfluoro-m-xylene with resorcinol or orcinol under mild conditions and subsequent heating of the mixture with 2,5-difluoro-4,6-bis(trifluoromethyl)benzene-1,3-dithiol leads to polyfluorinated dioxadithiacalix[4]arenes. Triphenyl and pentaphenyl ethers formed by the interaction of perfluoro-m-xylene with resorcinol under heating with thiourea gives polyfluorinated oxathiacalixarenes containing six and five aromatic nuclei, respectively. [ABSTRACT FROM AUTHOR]

Published
2021
Full Text
View/download PDF

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