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Original Articles

First liquid crystalline cuneane‐caged derivatives: a structure–property relationship study

, , , , , , & show all
Pages 689-696 | Accepted 15 Feb 2006, Published online: 20 Feb 2007

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R. J. Mandle, C. J. Gibb & J. L. Hobbs. (2024) Uncommon building blocks in liquid crystals. Liquid Crystals 0:0, pages 1-26.
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Articles from other publishers (7)

Yumiao Ma. (2024) Computational Research on Ag(I)-Catalyzed Cubane Rearrangement: Mechanism, Metal and Counteranion Effect, Ligand Engineering, and Post-Transition-State Desymmetrization. The Journal of Organic Chemistry 89:5, pages 3430-3440.
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Jeong-Yu Son, Santeri Aikonen, Nathan Morgan, Alexander S. Harmata, Jesse J. Sabatini, Rosario C. Sausa, Edward F. C. Byrd, Daniel H. Ess, Robert S. Paton & Corey R. J. Stephenson. (2023) Exploring Cuneanes as Potential Benzene Isosteres and Energetic Materials: Scope and Mechanistic Investigations into Regioselective Rearrangements from Cubanes. Journal of the American Chemical Society 145:30, pages 16355-16364.
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Elliot Smith, Kieran D. Jones, Luke O’Brien, Stephen P. Argent, Christophe Salome, Quentin Lefebvre, Alain Valery, Mina Böcü, Graham N. Newton & Hon Wai Lam. (2023) Silver(I)-Catalyzed Synthesis of Cuneanes from Cubanes and their Investigation as Isosteres. Journal of the American Chemical Society 145:30, pages 16365-16373.
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Adam Al‐Janabi & Richard J. Mandle. (2020) Utilising Saturated Hydrocarbon Isosteres of para Benzene in the Design of Twist‐Bend Nematic Liquid Crystals . ChemPhysChem 21:8, pages 697-701.
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Kyle F. Biegasiewicz, Justin R. Griffiths, G. Paul Savage, John Tsanaktsidis & Ronny Priefer. (2015) Cubane: 50 Years Later. Chemical Reviews 115:14, pages 6719-6745.
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Richard J. Mandle & John W. Goodby. 2014. Handbook of Liquid Crystals. Handbook of Liquid Crystals 1 39 .
Gábor Durkó & István Jalsovszky. (2013) Solvent-induced, selective rearrangement of hydrogen cubane-1,4-dicarboxylate to hydrogen cuneane-2,6-dicarboxylate. Tetrahedron 69:25, pages 5160-5163.
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