L-proline catalyzed an efficient multicomponent one -pot synthesis of poly substituted pyridines
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[1] T. Müller. Multicomponent reactions , 2011, Beilstein journal of organic chemistry.
[2] B. Narasimhan,et al. Synthesis and antitubercular activities of substituted benzoic acid N'-(substituted benzylidene/furan-2-ylmethylene)-N-(pyridine-3-carbonyl)-hydrazides. , 2010, European journal of medicinal chemistry.
[3] R. Calhelha,et al. Novel 6-[(hetero)arylamino]thieno[3,2-b]pyridines: synthesis and antitumoral activities. , 2010, European journal of medicinal chemistry.
[4] Shabana I. Khan,et al. Synthesis and the selective antifungal activity of 5,6,7,8-tetrahydroimidazo[1,2-a]pyridine derivatives. , 2010, European journal of medicinal chemistry.
[5] R. Butcher,et al. L-Proline-catalyzed one-pot expeditious synthesis of highly substituted pyridines at room temperature , 2010 .
[6] Y. Na,et al. Synthesis of 2-(thienyl-2-yl or -3-yl)-4-furyl-6-aryl pyridine derivatives and evaluation of their topoisomerase I and II inhibitory activity, cytotoxicity, and structure-activity relationship. , 2010, Bioorganic & medicinal chemistry.
[7] J. Zhou,et al. SYNTHESIS AND BIOLOGICAL EVALUATION OF 5,6-DIHYDRO-BENZO[C]ACRIDIN-7-OL DERIVATIVES AS ANTI-ALZHEIMERS DISEASE DRUGS , 2009 .
[8] Manish P. Patel,et al. One-Pot, Multicomponent Condensation Reaction in Neutral Conditions: Synthesis, Characterization, and Biological Studies of Fused Thiazolo[2,3-b]quinazolinone Derivatives , 2009 .
[9] A. Bishnoi,et al. Synthesis and Biological Evaluation of a Series of 4-(arylamido/imidoalkyl)- 5-(arylideno- 4-oxo-2-thio-imidazolidinyl)-N-(methyl-phenyl-imino) Acridinium Iodides as Potential Antiviral Agents , 2009 .
[10] P. Crooks,et al. Sulfamic acid catalyzed one‐pot synthesis of 2,5‐diaryl‐1,3,4‐oxadiazoles under microwave irradiation and conventional heating , 2009 .
[11] Cédric Kalinski,et al. Multicomponent Reactions asa Powerful Tool for Generic Drug Synthesis , 2008 .
[12] E. Novellino,et al. Design, synthesis, and structure-activity relationship studies of 4-quinolinyl- and 9-acrydinylhydrazones as potent antimalarial agents. , 2008, Journal of medicinal chemistry.
[13] Jurgen G Schmidt,et al. Multicomponent Reactions as a Powerful Tool for Generic Drug Synthesis Multicomponent Reactions for Generic Drug Synthesis , 2008 .
[14] J. Annereau,et al. Novel tetra-acridine derivatives as dual inhibitors of topoisomerase II and the human proteasome. , 2007, Biochemical pharmacology.
[15] Chaoguo Yan,et al. Microwave-assisted four-component, one-pot condensation reaction: an efficient synthesis of annulated pyridines. , 2007, Organic & biomolecular chemistry.
[16] Junyong Zhang,et al. An efficient and expeditious microwave-assisted synthesis of 4-azafluorenones via a multi-component reaction , 2007 .
[17] Junyong Zhang,et al. Kröhnke reaction in aqueous media: one-pot clean synthesis of 4′-aryl-2,2′:6′,2″-terpyridines , 2007 .
[18] B. Rajitha,et al. Sulfamic acid: a novel and efficient catalyst for the synthesis of aryl-14H-dibenzo[a.j]xanthenes under conventional heating and microwave irradiation , 2005 .
[19] Xianyong Wei,et al. An efficient improve for the kröhnke reaction : One-pot synthesis of 2,4,6-triarylpyridines using raw materials under microwave irradiation , 2005 .
[20] M. Yus,et al. Asymmetric multicomponent reactions (AMCRs): the new frontier. , 2005, Angewandte Chemie.
[21] Shu-Yun Cheng,et al. New analogues of AHMA as potential antitumor agents: synthesis and biological activity. , 2003, Bioorganic & medicinal chemistry.
[22] S. Martelli,et al. Rational design, synthesis and biological evaluation of thiadiazinoacridines: a new class of antitumor agents. , 2003, Bioorganic & medicinal chemistry.
[23] Yeh-long Chen,et al. Synthesis and antiinflammatory evaluation of 9-anilinoacridine and 9-phenoxyacridine derivatives. , 2002, Journal of medicinal chemistry.
[24] J. A. Spicer,et al. Synthesis and evaluation of unsymmetrical bis(arylcarboxamides) designed as topoisomerase-targeted anticancer drugs. , 2002, Bioorganic & medicinal chemistry.
[25] K. Erol,et al. 2-methyl-3-acetyl-4-aryl-5-oxo-1,4-dihydro-5H indeno(1,2-b) pyridine derivatives studies and their calcium antagonistic activities. , 1997, Bollettino chimico farmaceutico.
[26] Alan R. Katritzky,et al. Comprehensive Heterocyclic Chemistry IV , 1996 .
[27] F. Kroehnke. SYNTHESES USING PYRIDINIUM SALTS. 5. THE SPECIFIC SYNTHESIS OF PYRIDINES AND OLIGOPYRIDINES , 1976 .
[28] F. Kröhnke. The Specific Synthesis of Pyridines and Oligopyridines1 , 1976 .
[29] J. Barrio,et al. 2,4,6-Trisubstituted pyridines. Synthesis, fluorescence, and scintillator properties , 1973 .
[30] F. Kröhnke. Syntheses Using Pyridinium Salts (IV) , 1963 .
[31] F. Kröhnke,et al. Syntheses Using the Michael Adddition of Phridinium Salts , 1962 .