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RESEARCH PRODUCT
Derivatisation of Pyrogallarenes
Antti ÅHmanMinna LuostarinenChristoph A. SchalleyKari RissanenMaija Nissinensubject
AcylationOpen cavityHydrogen bondStereochemistryChemistryIntramolecular forceOrganic ChemistryCyclohexane conformationMoleculeRegioselectivityCrystal structurePhysical and Theoretical ChemistryMedicinal chemistrydescription
Derivatisation of upper-rim hydroxy groups of pyrogallarenes produced completely acylated and tosylated pyrogallarene derivatives. Mesitylation of pyrogallarene, however, resulted in a regioselective derivatisation of hydroxy groups, i.e. eight OH groups out of 12 were mesitylated. Crystal structures of the synthesised pyrogallarene derivatives indicate that completely substituted pyrogallarenes exist in a distorted crown conformation despite of the lack of stabilising intramolecular hydrogen bonds. In contrast, the partially substituted pyrogallarene adopts a boat conformation and has an open cavity for the inclusion of small guest molecules. © Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005)
year | journal | country | edition | language |
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2005-07-01 | European Journal of Organic Chemistry |