1.
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http://dx.doi.org/10.1016/j.bmc.2008.02.079Natural and non-natural prenylated chalcones: Synthesis, cytotoxicity and anti-oxidative activity
Susanne Vogela, Susanne Ohmayera, Gabi Brunnera and Jörg Heilmann
2.
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http://dx.doi.org/10.1016/j.catcom.2008.03.023Synthesis of chalcones via Claisen–Schmidt condensation reaction catalyzed by acyclic acidic ionic liquids
Fang Donga, Cheng Jiana, Fei Zhenghaob, Gong Kaia and Liu Zuliang
3.
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http://dx.doi.org/10.1016/S0223-5234(01)01245-4Synthesis of quinolinyl chalcones and evaluation of their antimalarial activity
José N. Domínguez, , a, Jaime E. Charrisa, Gricela Loboa, Neira Gamboa de Domínguezb, María M. Morenob, Flavia Riggionec, Erlinda Sanchezd, Jed Olsone and Philip J. Rosenthale
4.
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http://dx.doi.org/10.1016/S1350-4177(02)00079-2Improved synthesis of chalcones under ultrasound irradiation
Ji-Tai Li, Wen-Zhi Yang, Shu-Xiang Wang, Sheng-Hui Li and Tong-Shuang Li
5.
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http://dx.doi.org/10.1016/S0031-9422(02)00475-2Isolation and synthesis of chalcones with different degrees of saturation
Karsten Krohn, , Klaus Steingröver and M. Srinivasa Rao
6.
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http://dx.doi.org/10.1016/j.bmc.2009.02.052Solution-phase parallel synthesis of substituted chalcones and their antiparasitary activity against Giardia lamblia
Julio Montes-Avilaa, Sylvia P. Díaz-Camachob, Josefina Sicairos-Félixb, Francisco Delgado-Vargasb and I.A. Rivero
7.
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http://dx.doi.org/10.1016/j.bmcl.2008.01.112A new Heck reaction modification using ketone Mannich bases as enone precursors: Parallel synthesis of anti-leishmanial chalcones
Christina Reichwalda, Orly Shimonyb, Nina Sacerdoti-Sierrab, Charles L. Jaffeb and Conrad Kunick
8.
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http://dx.doi.org/10.1016/j.jcrysgro.2006.07.013Synthesis, crystal growth and studies on non-linear optical property of new chalcones
B.K. Sarojinia, , , B. Narayanab, B.V. Ashalathab, J. Indirac and K.G. Lobo
9.
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http://dx.doi.org/10.1016/j.ejmech.2005.05.008New syntheses and potential antimalarial activities of new retinoid-like chalcones
Alain Vallaa, Benoist Vallaa, Dominique Cartiera, Régis Le Guilloua, Roger Labiaa, Loic Florentb, Sébastien Charneaub, Joseph Schrevelb and Pierre Potierc
10.
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http://dx.doi.org/10.1016/j.bmcl.2008.10.126Synthesis and biological evaluation of a series of tangeretin-derived chalcones
Jérôme Quintina, Julie Desrivota, Sylviane Thoretb, Patrick Le Menezc, Thierry Cresteilb and Guy Lewin
11.
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http://dx.doi.org/10.1016/j.bmc.2007.10.039Synthesis and pharmacological activity of chalcones derived from 2,4,6-trimethoxyacetophenone in RAW 264.7 cells stimulated by LPS: Quantitative structure–activity relationships
Louise Domeneghini Chiaradiaa, Rodrigo dos Santosa, Carlos Eduardo Vitorb, André Alexandre Vieiraa, Paulo César Leala, Ricardo José Nunesa, João Batista Calixtob and Rosendo Augusto Yunes
12.
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http://dx.doi.org/10.1016/j.bmcl.2008.01.099Synthesis and biological evaluation of chalcones as inhibitors of the voltage-gated potassium channel Kv1.3
Julia Ciancia, b, Jonathan B. Baella, Bernard L. Flynnc, Robert, W. Gabled, Jorgen A. Mouldc, Dharam Paulc and Andrew J. Harvey
13.
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http://dx.doi.org/10.1016/j.ejmech.2006.12.014Acid-catalyzed synthesis of oxathiolone fused chalcones. Comparison of their activity toward various microorganisms and human cancer cells line
Marek T. Koniecznya, Wojciech Koniecznya, Michał Sabiszb, Andrzej Skladanowskib, Roland Wakiećb, Ewa Augustynowicz-Kopećc and Zofia Zwolska
14.
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http://dx.doi.org/10.1016/S0968-0896(99)00047-4Synthesis and screening of a combinatorial library of naphthalene substituted chalcones: inhibitors of leukotriene B4
Anil M. Deshpandea, Narshinha P. Argadea, Arvind A. Natua, and Joseph Eckman
15.
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http://dx.doi.org/10.1016/j.tet.2007.06.049Novel solid-supported dimerization–heteroannulation of chalcones: simple and efficient synthesis of 2,4,6-triaryl-3-methylarylpyridines
Anil K. Vermaa, Summon Koula, Ajay P.S. Pannub and Tej K. Razdan
16.
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http://dx.doi.org/10.1016/j.bmc.2008.04.026Design, synthesis, and biological evaluation of thiophene analogues of chalcones
Romeo Romagnoli, Pier Giovanni Baraldi, Maria Dora Carriona, Carlota Lopez Cara, Olga Cruz-Lopez, Delia Preti, Manlio Tolomeo, Stefania Grimaudo, Antonella Di Cristina, Nicola Zonta, Jan Balzarinid, Andrea Brancale, Taradas Sarkare and Ernest Hamel
17.
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http://dx.doi.org/10.1016/S0040-4020(01)00793-1Enantioselective conjugate addition of diethylzinc to chalcones catalysed by N-trityl aziridine-2-(S)-(diphenyl)methanol and Ni(acac)2
Uma Shadakshari and Sandip K. Nayak
18.
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http://dx.doi.org/10.1016/S0968-0896(99)00218-7Synthesis and biological activity of 4-alkoxy chalcones: potential hydrophobic modulators of p-glycoprotein-mediated multidrug resistance
Frédéric Boisa, Ahcène Boumendjel, Anne-Marie Mariottea, Gwenaëlle Conseilb and Attilio Di Petro
19.
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http://dx.doi.org/10.1016/j.tetlet.2007.03.054A simple and highly efficient method for the synthesis of chalcones by using borontrifluoride-etherate
T. Narender, and K. Papi Reddy
20.
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http://dx.doi.org/10.1016/j.ejmech.2008.05.010Examination of growth inhibitory properties of synthetic chalcones for which antibacterial activity was predicted
Daniela Batovska , Stoyan Parusheva, Bistra Stamboliyska, Iva Tsvetkova, Mariana Ninova and Hristo Najdenski
21.
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http://dx.doi.org/10.1016/S0166-1280(97)00274-1Synthesis and structure of 4-X-chalcones
L. J. Yamin, E. I. Gasull, S. E. Blanco and F. H. Ferretti
22.
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http://dx.doi.org/10.1016/j.catcom.2007.06.013SOCl2/EtOH: Catalytic system for synthesis of chalcones
Ognyan Petrov , Yordanka Ivanova and Mariana Gerova
23.
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http://dx.doi.org/10.1016/j.bmcl.2005.03.121Synthesis and biological evaluation of chalcones and their derived pyrazoles as potential cytotoxic agents
B.A. Bhata, K.L. Dhara, S.C. Puria, A.K. Saxenab, M. Shanmugavelb and G.N. Qazi
24.
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http://dx.doi.org/10.1016/j.ejmech.2007.05.006Synthesis, physicochemical properties and antimicrobial evaluation of new (E)-chalcones
Z. Nowakowska, B. Kędziab and G. Schroeder