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Original Articles

AN EFFICIENT SYNTHESIS OF 5-BROMO-2-HYDROXYCYCLOHEPTA-2, 4, 6-TRIEN-1-ONE AND ITS METHYL ETHER

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Pages 393-399 | Received 28 Jan 1988, Published online: 11 Feb 2009

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James Potenziano, Robert Spitale & Mark E. Janik. (2005) Improved and Highly Versatile Synthesis of 5‐Aryltropones. Synthetic Communications 35:15, pages 2005-2016.
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Ohki Sato, Ai Nitta & Ami Yamamoto. (2014) Regioselective Nucleophilic Substitution of 5-Bromo-2-methoxytropone. Heteroatom Chemistry 25:6, pages 644-650.
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Koji Takagi, Kazuhiro Saiki, Hirokazu Hayashi, Hiroyasu Ohsawa, Shin-ichi Matsuoka & Masato Suzuki. (2009) Tropolone-Terminated Oligomeric Fluorophores with Responsive Properties to External Environment. Bulletin of the Chemical Society of Japan 82:2, pages 236-241.
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Yoshihiro Miyake, Sayaka Watanabe, Satoshi Aono, Tohru Nishinaga, Akira Miyazaki, Toshiaki Enoki, Hitoshi Miyasaka, Hiroyuki Otani & Masahiko Iyoda. (2008) Long-distance ferromagnetic coupling through spin polarization in a linear heterotrinuclear iron(iii)–copper(ii)–iron(iii) complex derived from 5-ferrocenyl-2-aminotropone. Chemical Communications:46, pages 6167.
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Christopher J. Handy, Amy S. Manoso, William T. McElroy, W. Michael Seganish & Philip DeShong. (2005) Recent advances in siloxane-based aryl–aryl coupling reactions: focus on heteroaromatic systems. Tetrahedron 61:52, pages 12201-12225.
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W. Michael Seganish, Christopher J. Handy & Philip DeShong. (2005) Efforts Directed toward the Synthesis of Colchicine:  Application of Palladium-Catalyzed Siloxane Cross-Coupling Methodology. The Journal of Organic Chemistry 70:22, pages 8948-8955.
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Amy Morin Deveau & Timothy L. Macdonald. (2004) Practical synthesis of biaryl colchicinoids containing 3′,4′-catechol ether-based A-rings via Suzuki cross-coupling with ligandless palladium in water. Tetrahedron Letters 45:4, pages 803-807.
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M. G. BANWELL, J. N. LAMBERT, M. E. REUM & R. ONRUST. (1989) ChemInform Abstract: An Efficient Synthesis of 5-Bromo-2-hydroxycyclohepta-2,4,6-trien-1-one and Its Methyl Ether.. ChemInform 20:20.
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