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Pure Appl. Chem., 1999, Vol. 71, No. 2, pp. 265-273

http://dx.doi.org/10.1351/pac199971020265

Functional acetylenic molecular architecture

F. Diederich

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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>
  • Shoji Taku, Shimomura Erika, Maruyama Mitsuhisa, Ito Shunji, Okujima Tetsuo, Morita Noboru: Synthesis, Properties and Redox Behavior of Ene-Diyne Scaffolds Bearing 1- and 2-Azulenyl Groups at the Periphery. Eur. J. Org. Chem. 2013, 2013, 957. <http://dx.doi.org/10.1002/ejoc.201201397>
  • Shoji Taku, Ito Shunji, Okujima Tetsuo, Morita Noboru: Synthesis and [2+2] Cycloaddition with Tetracyanoethylene of Ene-Diyne Scaffolds Bearing Ferrocenes at the Periphery. Eur J Org Chem 2011, 2011, 5134. <http://dx.doi.org/10.1002/ejoc.201100650>
  • Diederich Francois: ChemInform Abstract: Functional Acetylenic Molecular Architecture. ChemInform 2010, 31, no. <http://dx.doi.org/10.1002/chin.200002299>
  • Ito Shunji, Morita Noboru: Creation of Stabilized Electrochromic Materials by Taking Advantage of Azulene Skeletons. Eur J Org Chem 2009, 2009, 4567. <http://dx.doi.org/10.1002/ejoc.200900393>
  • Ito Shunji, Iida Takahiro, Kawakami Jun, Okujima Tetsuo, Morita Noboru: Towards the Preparation of Electrochromic Materials with Strong Absorption in the Near-Infrared Region: Synthesis and Redox Behavior of Azulene-Substituted Enediyne Scaffolds Connected by a 9,10-Anthracenediyl Spacer. Eur J Org Chem 2009, 2009, 5355. <http://dx.doi.org/10.1002/ejoc.200900743>
  • Shoji Taku, Ito Shunji, Toyota Kozo, Morita Noboru: Synthesis and redox behavior of ene–diyne scaffolds that bear ferrocenes at the periphery. Tetrahetron Lett 2009, 50, 2825. <http://dx.doi.org/10.1016/j.tetlet.2009.03.172>
  • Koentjoro Olivia F, Zuber Philipp, Puschmann Horst, Goeta Andres E, Howard Judith A.K, Low Paul J: A simple synthesis of tetraethynylethenes and representative molecular structures of some dicobalt derivatives. J Organomet Chem 2003, 670, 178. <http://dx.doi.org/10.1016/S0022-328X(02)02191-5>
  • Hopf Henning, Kämpen Jan, Bubenitschek Peter, Jones Peter G.: En Route to 7,7,8,8-Tetraethynyl-p-quinodimethane (TEQ). Eur J Org Chem 2002, 2002, 1708. <http://dx.doi.org/10.1002/1099-0690(200205)2002:10<1708::AID-EJOC1708>3.0.CO;2-A>
  • Maurette Luc, Godard Cyril, Frau Silvana, Lepetit Christine, Soleilhavoup Michèle, Chauvin Remi: On Ring Carbomers of Cyclobutane, Cyclopentane, and Cyclodecane and Cyclization Reactions through Bis(alkynyl-propargyl) Coupling. Chem Eur J 2001, 7, 1165. <http://dx.doi.org/10.1002/1521-3765(20010316)7:6<1165::AID-CHEM1165>3.0.CO;2-3>