Conformational properties of cyanomethoxy calix[4]arenes.

Abstract

O-Alkylation of the dinitro calix[4]arene 2, easily available by selective ipso-nitration of the di-cyanomethyl ether 1, with allylbromide (DMF/Cs2CO3) gave tetraethers 3 and 4 with anti- and syn-orientations of the two allyl ether residues. The two possible stereoisomers of in the partial cone and 1,2-alternate conformation exist as an equilibrium mixture… (More)

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Cite this paper

@article{Danila2005ConformationalPO, title={Conformational properties of cyanomethoxy calix[4]arenes.}, author={Crenguta Danila and Volker B{\"{o}hmer and Michael Bolte}, journal={Organic & biomolecular chemistry}, year={2005}, volume={3 19}, pages={3508-13} }