[1] Kasende O E,Muya J T,Broeckaert L,et al. Theoretical Study of the Regioselectivity of the Interaction of 3-Methyl-4-pyrimidone and 1-Methyl-2-pyrimidone with Lewis Acids[J]. J Phys Chem A,2012,116:8608-8614.[2] Aslam M,Verma S. Biological Activity of Newly Synthesized Substituted Dihydropyrimidinone and Thione[J]. Int J Chem Tech Res,2012,4(1):109-111.[3] Jayakumar S,Shabeer T K. Multicomponent Biginelli Synthesis of 3,4-Dihydropyrimidin-2(1H)-ones by Grindstone Technique and Evaluation of Their Biological Properties[J]. J Chem Pharm Res,2011,3(6):1089-1096.[4] LIU Ju,JING Chunyan,WANG Yang,et al. Synthesis of 3,6-Diarylpyrazolo[1,5-a] pyrimidines[J]. Chinese J Appl Chem,2013,30(12):1494-1496(in Chinese).刘举,敬春艳,汪洋,等. 新型3,6-二芳基吡唑并[1,5-a]嘧啶类化合物的合成[J]. 应用化学,2013,30(12):1494-1496.[5] XIAO Liwei. Synthesis of 2-Substituted Aryl Benzoxazoles Catalyzed by Ammonium Metavanadate[J]. Chinese J Org Chem,2011,31(6):878-880(in Chinese).肖立伟. 偏钒酸铵催化合成2-芳基取代苯并噁唑[J]. 有机化学,2011,31(6):878-880.[6] LUO Dong,GAO Meixiang,MAO Liqiu,et al. Oxidation of Cyclohexylamine to Cyclohexanone Oxime Catalyzed by NaY Zeolite Moledular Sieves[J]. Chinese J Appl Chem,2013,30(12):1443-1448(in Chinese).罗东,高美香,毛丽秋,等. NaY型沸石分子筛催化环己胺氧化制备环己酮肟[J]. 应用化学,2013,30(12):1443-1448.[7] Fan X S,Wang Y Y,Qu Y Y,et al. Tandem Reactions Leading to Bicyclic Pyrimidine Nucleosides and Benzopyran-4-ones[J]. J Org Chem,2011,76(3):982-985.[8] Dalinger I L,Vatsadse I A,Shevelev S A,et al. Liquid-phase Synthesis of Combinatorial Libraries Based on 7-Trifluoromethyl-substituted Pyrazolo[1,5-a] pyrimidine Scaffold[J]. J Comb Chem,2005,7(2):236-245.[9] Marcotte F A,Rombouts F J R and Lubell W D. Diversity-oriented Synthesis of Functionalized Pyrrolo[3,2-d] pyrimidines with Variation of the Pyrimidine Ring Nitrogen Substituents[J]. J Org Chem,2003,68(18):6984-6987.[10] Iwai S,Shimizu M,Kamiya H,et al. Synthesis of a Phosphoramidite Coupling Unit of the Pyrimidine(6-4) pyrimidone Photoproduct and Its Incorporation into Oligodeoxynucleotides[J]. J Am Chem Soc,1996,118(32):7642-7643.[11] Beck J R,Yahner J A. Synthesis of [l] Benzothieno[3,2-d] pyrirnidine Derivatives[J]. J Org Chem,1973,38(14):2450-2452.[12] Joseph J K,Jain S L,Singhal S,et al. Efficient Synthesis of 3,4-Dihydropyrimidinones in 1-n-Butyl-3-methylimidazolium Tetrachloroindate (BMI InCl4)[J]. Ind Eng Chem Res,2011,50:11463-11466.[13] YANG Shuijin,TONG Wenlong. Synthesis of 4-Phenyl-6-methyl-5-ethoxycarbonyl-3,4-dihydropyrimidin-2(H)-one Catalyzed with H3PW6Mo6O40[J]. Chem Intermed,2007,(1):22-24(in Chinese).杨水金,童文龙. 磷钨钼酸催化合成4-苯基-6-甲基-5-乙氧羰基-3,4-二氢嘧啶-2(H)-酮[J]. 化工中间体,2007,(1):22-24.[14] Bhorodwaj S K,Dutta D K. Heteropoly Acid Supported Modified Montmorillonite Clay:an Effective Catalyst for the Esterification of Acetic Acid with Sec-butanol[J]. Appl Catal A:Gen,2010,378(2,30):221-226.[15] Izumi Y,Hisano K,Hida T. Acid Catalysis of Silica-included Heteropolyacid in Polar Reaction Media[J]. Appl Catal A:Gen,1999,181:277-282.[16] Yu L,Huang Y K,Duan G B,et al. Catalytic Synthesis of n-Butyl Methacrylate with H4SiW6Mo6O40/SiO2[J]. Adv Mater Res,2013,631/632:135-139.[17] Izumi Y,Ono M,Kitagawa M,et al. Silica-included Heteropoly Compounds as Solid Acid Catalysts[J]. Micropor Mat,1995,5(4):255-262.[18] Jermy B R,Pandurangan A. Synthesis of Geminal Diacetates(Acylals) Using Heterogeneous H3PW12O40 Supported MCM-41 Molecular Sieves[J]. Catal Commun,2008,9(5):577-583.[19] Sui C H,Li C,Guo X H,et al. Facile Synthesis of Silver Nanoparticles-modified PVA/H4SiW12O40 Nanofibers-based Electrospinning to Enhance Photocatalytic Activity[J]. Appl Surf Sci,2012,258(18):7105-7111.[20] Yang S J,Xu Y L,Huang Y K,et al. Photocatalytic Degradation of Methyl Violet with TiSiW12O40/TiO2[J]. Int J Photoenergy,2013,Article ID 191340.[21] Lei P X,Chen C C,Yang J,et al. Degradation of Dye Pollutants by Immobilized Polyoxometalate with H2O2 Under Visible-Light Irradiation[J]. Environ Sci Technol,2005,39(21):8466-8474.[22] Sepúlveda J H,Yori J C,Vera C R. Repeated use of Supported H3PW12O40 Catalysts in the Liquid Phase Esterification of Acetic Acid with Butanol[J]. Appl Catal A:Gen,2005,288(1/2):18-24.[23] YU Fuchao,YAN Shengjiao,LIN Jun. Application of Solvent-Free Reaction in Synthesis of Heterocyclic Compounds[J]. Chinese J Org Chem,2010,30(10):1421-1430(in Chinese).余富朝,严胜骄,林军. 无溶剂反应在杂环合成中的应用进展[J]. 有机化学,2010,30(10):1421-1430.[24] Chowdhury S,Nandi G C,Samai S,et al. Regioselective Synthesis of Tetrahydrothiochromen-5-ones via a One-Pot Three-Component Solvent-Free Domino Protocol[J]. Org Lett,2011,13(14):3762-3765.[25] XIAO Liwei,LI Huizhang,LIU Huimin,et al. Knoevenagel Condensation in Solvent Free Condition Under Microwave Irradiation[J]. J Hebei Univ(Nat Sci),2003,23(2):167-169(in Chinese).肖立伟,李慧章,刘卉闵,等. 无溶剂微波辐射下的Knoevenagel缩合反应[J]. 河北大学学报(自然科学版),2003,23(2):167-169. |