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Pure Appl. Chem., 2008, Vol. 80, No. 3, pp. 621-637

http://dx.doi.org/10.1351/pac200880030621

Expanded radialenes: Modular synthesis and properties of cross-conjugated enyne macrocycles

Rik R. Tykwinski1, Mojtaba Gholami1, Sara Eisler1, Yuming Zhao2, Frederic Melin3 and Luis Echegoyen3

1 Department of Chemistry, University of Alberta, Edmonton, Alberta T6G 2G2, Canada
2 Department of Chemistry, Memorial University of Newfoundland, St. John's, NL A1B 3X7, Canada
3 Department of Chemistry, Clemson University, Clemson, SC 29634, USA

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  • Gholami Mojtaba, Ramsaywack Sharwatie, Chaur Manuel N., Murray Adrian H., McDonald Robert, Ferguson Michael J., Echegoyen Luis, Tykwinski Rik R.: Synthesis and Derivatization of Expanded [n ]Radialenes (n =3, 4). Chem. Eur. J. 2013, 19, 15120. <http://dx.doi.org/10.1002/chem.201302452>
  • Dutta Tanmoy, Che Yanke, Zhong Haizhen, Laity John H., Dusevich Vladimir, Murowchick James B., Zang Ling, Peng Zhonghua: Synthesis and self-assembly of triphenylene-containing conjugated macrocycles. RSC Adv. 2013, 3, 6008. <http://dx.doi.org/10.1039/c3ra23421e>
  • Mackay Emily G., Sherburn Michael S.: Demystifying the dendralenes. Pure Appl. Chem. 2013, 1. <http://dx.doi.org/10.1351/PAC-CON-13-02-04>
  • Hopf Henning, Sherburn Michael S.: Dendralene auf dem Vormarsch: kreuzkonjugierte Oligoene ermöglichen den schnellen Aufbau molekularer Komplexität. angew chemie 2012, 124, 2346. <http://dx.doi.org/10.1002/ange.201102987>
  • Hopf Henning, Sherburn Michael S.: Dendralenes Branch Out: Cross-Conjugated Oligoenes Allow the Rapid Generation of Molecular Complexity. Angew Chem Int E 2012, 51, 2298. <http://dx.doi.org/10.1002/anie.201102987>
  • Chen Pangkuan, Jäkle Frieder: Highly Luminescent, Electron-Deficient Bora-cyclophanes. S J Am Chem Soc 2011, 133, 20142. <http://dx.doi.org/10.1021/ja209602z>
  • Diederich François, Kivala Milan: All-Carbon Scaffolds by Rational Design. Adv Mater 2010, 22, 803. <http://dx.doi.org/10.1002/adma.200902623>
  • Shopsowitz Kevin E., Edwards David, Gallant Amanda J., MacLachlan Mark J.: Highly substituted Schiff base macrocycles via hexasubstituted benzene: a convenient double Duff formylation of catechol derivatives. Tetrahedron 2009, 65, 8113. <http://dx.doi.org/10.1016/j.tet.2009.07.094>
  • Zhu Yuan-Yuan, Wang Gui-Tao, Li Zhan-Ting: A click chemistry approach for the synthesis of macrocycles from aryl amide-based precursors directed by hydrogen bonding. Org Biomol Chem 2009, 7, 3243. <http://dx.doi.org/10.1039/b907457k>
  • Tykwinski Rik R., Gholami Mojtaba, Eisler Sara, Zhao Yuming, Melin Frederic, Echegoyen Luis: ChemInform Abstract: Expanded Radialenes: Modular Synthesis and Properties of Cross-Conjugated Enyne Macrocycles. ChemInform 2008, 39. <http://dx.doi.org/10.1002/chin.200830256>