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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 32, 2002 - Issue 2
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Original Articles

SOLID-PHASE SYNTHESIS OF FERROCENYLCHALKONE

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Pages 171-174 | Received 15 Feb 2000, Published online: 16 Aug 2006

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A. Chakradhar, R. Roopa, K. C. Rajanna & P. K. Saiprakash. (2009) Vilsmeier–Haack Bromination of Aromatic Compounds with KBr and N-Bromosuccinimide Under Solvent-Free Conditions. Synthetic Communications 39:10, pages 1817-1824.
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Yinjuan Bai, Jun Lu, Haiying Gan, Zhenjun Wang & Zhen Shi. (2004) Green Chemistry Approaches to Condensation Reactions of Formylferrocene with Active Methylene Containing Compounds. Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry 34:8, pages 1487-1496.
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Articles from other publishers (12)

Ingrid Montes-González, Ambar M. Alsina-Sánchez, Juan C. Aponte-Santini, Sara M. Delgado-Rivera & Geraldo L. Durán-Camacho. (2019) Perspectives of ferrocenyl chalcones: synthetic scaffolds toward biomedical and materials science applications. Pure and Applied Chemistry 91:4, pages 653-669.
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Sara M. Delgado-Rivera, Giovanny E. Pérez-Ortiz, Andrés Molina-Villarino, Fabiel Morales-Fontán, Lyannis M. García-Santos, Alma M. González-Albó, Ana R. Guadalupe & Ingrid Montes-González. (2017) Synthesis and characterization of novel ferrocenyl chalcone ammonium and pyridinium salt derivatives. Inorganica Chimica Acta 468, pages 245-251.
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Guillermo Ahumada, Paul Hamon, Vincent Dorcet, Thierry Roisnel, Carolina Manzur, David Carrillo, Juan Pablo Soto & Jean-René Hamon. (2013) Two substrates, three products: Reactions between ferrocene-carboxaldehyde and dioxaphospholene, characterization and crystal structures of oxygenated C3- and C4-chain-containing ferrocenes. Journal of Organometallic Chemistry 732, pages 40-46.
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Bing Wei, Yong Gao, Cai-Xia Lin, Heng-Dong Li, Li-Li Xie & Yao-Feng Yuan. (2011) Synthesis, structure and electrochemical behaviour of 2,2-diferrocenylpropane-substituted dihydropyrazole derivatives. Journal of Organometallic Chemistry 696:8, pages 1574-1578.
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A.R. Sureshbabu, R. Raghunathan & B.K. Satiskumar. (2009) A facile synthesis of ferrocene grafted N-methyl-spiropyrrolidines through 1,3-dipolar cycloaddition of azomethine ylides. Tetrahedron Letters 50:23, pages 2818-2821.
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Andrea-Nekane Alba, Pilar Gómez-Sal, Ramon Rios & Albert Moyano. (2009) Organocatalytic kinetic resolution of a planar-chiral ferrocenecarbaldehyde. Tetrahedron: Asymmetry 20:11, pages 1314-1318.
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YounJung Jung, Kyung-In Son, Youl Eui Oh & Dong-Youn Noh. (2008) Ferrocenyl chalcones containing anthracenyl group: Synthesis, X-ray crystal structures and electrochemical properties. Polyhedron 27:2, pages 861-867.
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Kyung-In Son & Dong-Youn Noh. (2007) Solvent-free Synthesis, X-ray Structure Analysis and Electrochemical Properties of Ferrocenylchalcone containing Naphtalenyl Group. Journal of the Korean Chemical Society 51:6, pages 591-594.
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Christopher Imrie, Phumelele Kleyi, Vincent O. Nyamori, Thomas I.A. Gerber, Demetrius C. Levendis & Jennifer Look. (2007) Further solvent-free reactions of ferrocenylaldehydes: Synthesis of 1,1′-ferrocenyldiimines and ferrocenylacrylonitriles. Journal of Organometallic Chemistry 692:16, pages 3443-3453.
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Christopher Imrie, Elago R.T. Elago, Nadia Williams, Cedric W. McCleland & Pieter Engelbrecht. (2005) Synthesis of ferrocenoate esters, amides and other ferrocenoyl derivatives using ferrocenoyl fluoride. A comparison of the reactions of ferrocenoyl fluoride in [bmim][BF4] with the microwave-promoted solvent-free reactions of ferrocenoyl fluoride. Journal of Organometallic Chemistry 690:21-22, pages 4959-4966.
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Wan‐yi Liu, Qi‐hai Xu, Bao‐hua Chen & Yong‐xiang Ma. (2010) ChemInform Abstract: Solid‐Phase Synthesis of Ferrocenylchalkone.. ChemInform 33:25.
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Wan-yi Liu, Qi-hai Xu, Bao-hua Chen, Yong-min Liang, Yong-xiang Ma & Wei-min Liu. (2001) Preparation of ferrocenyl mono- and dienone derivatives through aldol condensation of 1,1′-diacetylferrocene with aromatic aldehydes in dry conditions. Journal of Organometallic Chemistry 637-639, pages 782-785.
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