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O. Hayashida and T. Nakashima, “Synthesis of Cyclophane Dimer Using Cyclophane-Tethered Fmoc-Amino Acid Derivatives as a Multivalent Host,” Chemistry Letters, Vol. 40, No. 2, 2011, pp. 134-135. doi:10.1246/cl.2011.134

has been cited by the following article:

• TITLE: Synthesis and Enhanced Guest-Binding Affinities of Dendrimer-Based Cyclophane Tetramer and Octamer

  AUTHORS: Osamu Hayashida, Tomomi Nakashima, Yu Kaku

  KEYWORDS: Cyclophane Oligomer; Host-Guest Chemistry; Multivalency Effect

  JOURNAL NAME: Advances in Chemical Engineering and Science, Vol.3 No.3A1, July 15, 2013

  ABSTRACT: Dendritic cyclophane tetramer and octamer were prepared by aminolysis of succinimidyl ester derivative of tetraaza [6.1.6.1] paracyclophane with the corresponding poly(amidoamine) dendrimers as a scaffold, followed by removal of the protecting groups. The present cyclophane tetramer and octamer showed enhanced guest-binding affinities toward fluorescent guests such as 6-p-toluidinonaphthalene-2-sulfonate and 6-anilinonaphthalene-2-sulfonate, in comparison with those of monocyclic cyclophane, reflecting multivalency effects in macrocycles.