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Collect. Czech. Chem. Commun. 2004, 69, 1325-1344
https://doi.org/10.1135/cccc20041325

Concave Reagents. New 2'-Substituted m-Terphenyls

Michael Abbassa, Christine Kühlb, Christian Mantheyc, Anja Müllerd and Ulrich Lüninge,*

a ChemCon GmbH, Engesserstrasse 4b, D-79108 Freiburg, Germany
b Bernina Biosystems GmbH, Am Klopferspitz 19a, D-82152 Martinsried, Germany
c ipal Gesellschaft für Patentverwertung Berlin mbH, Bundesallee 210, D-10719 Berlin, Germany
d Gilson International BV, Otto-Hahn-Str. 17, D-65520 Bad Camberg, Germany
e Institut für Organische Chemie, Olshausenstr. 3/4, D-24098 Kiel, Germany

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  • Kole Priyanka B., Sakthivel Kokila, Armaković Sanja J., Armaković Stevan, Iqbal Muzaffar, Singh Fateh V., Kollur Shiva Prasad: Metal free synthesis of thermally stable blue fluorescent m-terphenyls by ring transformation of 2H-pyran-2-ones: chemical synthesis, spectroscopy and computational studies. RSC Adv. 2024, 14, 16960. <https://doi.org/10.1039/D4RA02375G>
  • Thirunarayanan Ayyavu, Raja Sebastian, Mohanraj Gunasekaran, Rajakumar Perumal: Synthesis of chiral core based triazole dendrimers with m-terphenyl surface unit and their antibacterial studies. RSC Adv. 2014, 4, 41778. <https://doi.org/10.1039/C4RA04967E>
  • Dickie Diane A, MacIntosh Ian S, Ino Daisuke D, He Qi, Labeodan Ojisamola A, Jennings Michael C, Schatte Gabriele, Walsby Charles J, Clyburne Jason A.C.: Synthesis of the bulky m-terphenyl phenol Ar*OH (Ar* = C6H3-2,6-Mes2, Mes = 2,4,6-trimethylphenyl) and the preparation and structural characterization of several of its metal complexes. Can. J. Chem. 2008, 86, 20. <https://doi.org/10.1139/v07-131>
  • Abbass Michael, Kuehl Christine, Manthey Christian, Mueller Anja, Luening Ulrich: Concave Reagents. Part 42. New 2′‐Substituted m‐Terphenyls. ChemInform 2004, 35. <https://doi.org/10.1002/chin.200443093>