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Please use this identifier to cite or link to this item: http://eprint.iitd.ac.in/handle/2074/1065

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dc.contributor.authorArora, Vandna-
dc.contributor.authorChawla, H M-
dc.contributor.authorSantra, Anuradha-
dc.date.accessioned2005-12-30T04:22:35Z-
dc.date.available2005-12-30T04:22:35Z-
dc.date.issued2002-
dc.identifier.citationTetrahedron, 58(28), 5591-5597en
dc.identifier.urihttp://eprint.iitd.ac.in/dspace/handle/2074/1065-
dc.description.abstractBy careful choice of a catalyst (TiCl4 or SnCl4), temperature, reaction time and mole ratio of the substrate to dichloromethylmethylether, it has been possible to obtain new functionalized formylated calix[n]arenes in the cone or partial cone conformation. Optimized general reaction procedures for obtaining mono-, di-, tri- and tetraformylated derivatives of calix[4]arenes as exemplified by formylation of tetramethoxy-, tetrakis(2-ethoxyethoxy)-, bis(ethoxycarbonylmethoxy)- and bis(hexadecyloxy)-calix[4]-arenes have been reported.en
dc.format.extent71142 bytes-
dc.format.mimetypeapplication/pdf-
dc.language.isoenen
dc.subjectselectiveen
dc.subjectcalix[4]areneen
dc.subjectformylationen
dc.titleSynthesis of selectively formylated calixarene ethersen
dc.typeArticleen
Appears in Collections:Chemistry

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