The synthesis of the first family of fully substituted cucurbit[<i>n</i>]uril is discussed, and the structural features of precursor glycolurils are highlighted in their importance to achieving higher homologues. The members of the family, where <i>n</i> = 5–7, have been fully characterized, and increased binding affinities have been identified for dioxane in CyP<sub>6</sub>Q[6] and adamantyl NH<sub>3</sub><sup>+</sup> in CyP<sub>7</sub>Q[7]. A higher homologue is indicated but not conclusively identified
A novel approach to cucurbituril synthesis is described where partial substitution is introduced int...
A novel approach to cucurbituril synthesis is described where partial substitution is introduced int...
The selectivity and recognition behavior of cucurbit[n]uril (CB[n]) homologues (n=6,7,8) towards a d...
The synthesis of the first family of fully substituted cucurbit[<i>n</i>]uril is discussed, and th...
The synthesis of the first family of fully substituted cucurbit[<i>n</i>]uril is discussed, and th...
The synthesis of the first family of fully substituted cucurbit[<i>n</i>]uril is discussed, and th...
The cucurbit[n]uril (Q[n]) family provides real potential for a wide range of applications, includin...
Classical cucurbit[n]uril (Q[n], n = 5 to 10) are macrocyclic structures resembling a hollow pumpkin...
The supramolecular chemistry of cucurbituril, a synthetic receptor, is fascinating because of the re...
The successful formation of higher homologues in the case of the fully substituted CyPnQ[n] from a g...
The cucurbit[n]uril family is an attractive molecular host, due to its molecular guest binding prope...
The recently discovered cucurbit[n]uril are a range of macrocyclic hosts which have enormous potenti...
Two new glycoluril diethers have been prepared, bearing strained cyclobutene and cyclobutane rings a...
Cucurbit[n]uril, CB[n], is made from the condensation of glycoluril and formaldehyde in concentrated...
The set of molecules cucurbit[n]uril (Qn) are macrocycles composed of n glycolurilmonomers linked by...
A novel approach to cucurbituril synthesis is described where partial substitution is introduced int...
A novel approach to cucurbituril synthesis is described where partial substitution is introduced int...
The selectivity and recognition behavior of cucurbit[n]uril (CB[n]) homologues (n=6,7,8) towards a d...
The synthesis of the first family of fully substituted cucurbit[<i>n</i>]uril is discussed, and th...
The synthesis of the first family of fully substituted cucurbit[<i>n</i>]uril is discussed, and th...
The synthesis of the first family of fully substituted cucurbit[<i>n</i>]uril is discussed, and th...
The cucurbit[n]uril (Q[n]) family provides real potential for a wide range of applications, includin...
Classical cucurbit[n]uril (Q[n], n = 5 to 10) are macrocyclic structures resembling a hollow pumpkin...
The supramolecular chemistry of cucurbituril, a synthetic receptor, is fascinating because of the re...
The successful formation of higher homologues in the case of the fully substituted CyPnQ[n] from a g...
The cucurbit[n]uril family is an attractive molecular host, due to its molecular guest binding prope...
The recently discovered cucurbit[n]uril are a range of macrocyclic hosts which have enormous potenti...
Two new glycoluril diethers have been prepared, bearing strained cyclobutene and cyclobutane rings a...
Cucurbit[n]uril, CB[n], is made from the condensation of glycoluril and formaldehyde in concentrated...
The set of molecules cucurbit[n]uril (Qn) are macrocycles composed of n glycolurilmonomers linked by...
A novel approach to cucurbituril synthesis is described where partial substitution is introduced int...
A novel approach to cucurbituril synthesis is described where partial substitution is introduced int...
The selectivity and recognition behavior of cucurbit[n]uril (CB[n]) homologues (n=6,7,8) towards a d...