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140Christof SchonThese authors contributed equally, Wolfgang Roth, Ingo Fischer, Johannes Pfister, Conrad Kaiser, Reinhold F. Fink and Bernd Engels.
Paracyclophanes as model compounds for strongly interacting π-systems. Part 1. Pseudo-ortho-dihydroxy[2.2]paracyclophane, Phys. Chem. Chem. Phys., 2010, 12, 9339. Richard J. Seacome, Martyn P. Coles, Jean E. Glover, Peter B. Hitchcock and Gareth J. Rowlands.
Planar-chiral imidazole-based phosphine ligands derived from [2.2]paracyclophaneCCDC reference numbers 753893–753896. For crystallographic data in CIF or other electronic format see DOI: 10.1039/b923716j, Dalton Trans., 2010, 39, 3687. I. Dix, H. Hopf, P.G. Jones.
Heterocycle-substituted [2.2]paracyclophanes, Acta Cryst C 1999 Volume 55 Part 5 Page 756-759 Luca Valentini, Aldo Taticchi, Assunta Marrocchi and Josè M. Kenny.
Patterning of [2.2]paracyclophane derivative modified single-walled carbon nanotubes through grid-assisted deposition, J. Mater. Chem., 2008, 18, 484. Gareth J. Rowlands.
The synthesis of enantiomerically pure [2.2]paracyclophane derivatives, Org. Biomol. Chem., 2008, 6, 1527. Kazumasa Kanda, Tamami Koike, Kohei Endo and Takanori Shibata.
The first asymmetric Sonogashira coupling for the enantioselective generation of planar chirality in paracyclophanes, Chem. Commun., 2009, 1870. Jeremy K. Klosterman, Yoshihiro Yamauchi and Makoto Fujita.
Engineering discrete stacks of aromatic molecules, Chem. Soc. Rev., 2009, 38, 1714. Jiwu Ruan, Lee Shearer, Jun Mo, John Bacsa, Antonio Zanotti-Gerosa, Fred Hancock, Xiaofeng Wu and Jianliang Xiao.
[2.2]Paracyclophane-based monophosphine ligand for palladium-catalyzed cross-coupling reactions of aryl chlorides, Org. Biomol. Chem., 2009, 7, 3236. Katsuya Mutoh and Jiro Abe.
Photochromism of a water-soluble vesicular [2.2]paracyclophane-bridged imidazole dimer, Chem. Commun., 2011, 47, 8868.