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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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'Twisted' isophthalamide analogues.

Steric interactions in 1,3-dicarboxamidoanthraquinones have been employed to 'twist' isophthalamide-like anion binding sites; the crystal structure of the fluoride complex of a bis-3,5-dichlorophenylamide derivative shows the receptor acting as a 'hydrogen-bonding corner' in a '2 + 2' fluoride containing molecular box.[1]

References

  1. 'Twisted' isophthalamide analogues. Brooks, S.J., Evans, L.S., Gale, P.A., Hursthouse, M.B., Light, M.E. Chem. Commun. (Camb.) (2005) [Pubmed]
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