毕业论文

打赏
当前位置: 毕业论文 > 研究现状 >

喹啉类化合物的合成研究现状和参考文献(2)

时间:2021-01-16 14:24来源:毕业论文
[13] Nayak J, Girisha KS, Shetty NS, et al. Synthesis of some 1,3,4-thiadiazolescarrying quinoline moiety as possible bioactive agents [J]. Indian J Heterocyc Chem,2008, 17: 209-212. [14] Yu ZY, Shi G

[13] Nayak J, Girisha KS, Shetty NS, et al. Synthesis of some 1,3,4-thiadiazolescarrying quinoline moiety as possible bioactive agents [J]. Indian J Heterocyc Chem,2008, 17: 209-212.

[14] Yu ZY, Shi GY, Sun Q, et al. Design, synthesis and in vitro antibacterial /antifungal evaluation of novel 1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7(1-piperazinyl)quinoline -3-carboxylic acid derivatives[J]. Eur J Med Chem, 2009, 44: 4726-4733.[15] Tseng CH, Tzeng CC, Yang CL, et al. Synthesis and antiproliferative evaluationof certain indeno [1,2-c] quinolone derivatives. part 2 [J]. J Med Chem, 2010, 53:6164-6179.

[16] Chakrabarty M, Mukherji A, Karmakar S, et al. An expedient synthesis of novel2-substituted thiazolo [4,5-f]isoquinolines /quinolines and benzo [1,2-d:4,3-d’]bisthiazoles and their potential as inhibitors of COX -1 and COX -2 [J]. Arkivoc,2010, 265-290.

[17] O’ Donnell F, Smyth TJP, Ramachandran VN, et al. A study of the antimicrobialactivity of selected synthetic and naturally occurring quinolines [J]. Int J Antimicrob,Agents, 2010, 35: 30-38.

[18] Singh S, Kumar V, Kumar A, et al. A Study of antibacterial activity of somenovel 8-methoxy-4-methyl-quinoline derivatives[J]. Bull Korean Chem Soc, 2010,31(12): 3605-3610.

[19] Nien CY, Chen YC, Kuo CC, et al. 5-Amino-2-aroylquinolines as highly potenttubulin polymerization inhibitors[J]. J Med Chem, 2010, 53: 2309-2313.

[20] Hosokawa T, Matsumura A, Katagiri T, et al. One-pot synthesis of 3-fluoro-4-(trifluoromethyl)quinolines from pentafluoropropen-2-ol and their molecular

modification [J]. J Org Chem, 2008, 73: 1468-1474.

[21] Akbari J, Heydari A, Kalhor HR, et al. Sulfonic acid functionalized ionic liquidin combinatorial approach, a recyclable and water tolerant-acidic catalyst for one-potfriedlander quinoline synthesis [J]. J Comb Chem, 2010, 12: 137-140.

[22] Dabiri M, Salehi P, Bahramnejad M, et al. Synthesis of diheterocycliccompounds based on triazolyl methoxy phenylquinazolines via a one-Potfour-component-click reaction[J]. J Comb Chem, 2010, 12: 638-642.

[23] Mali JR, Pratap UR, Jawale DV, et al. Water-mediated one -pot synthetic routefor pyrazolo [3,4-b]quinolines [J].Tetrahedron Lett, 2010, 51: 3980-3982.

[24] Jwanro Hassan, Marc Se´vignon, Christel Gozzi, Emmanuelle Schulz, and Marc Lemaire*.Aryl-Aryl Bond Formation One Century after the Discovery of the Ullmann Reaction.,2002, 102, 1359-1469

[25] 廖开胜. 一锅法合成以S-S键结合的氮杂环丁烷及萘并呋喃衍生物的方法学研究. 安徽师范大学, 化学世界, 2011(5): 303-305

 


喹啉类化合物的合成研究现状和参考文献(2):http://www.751com.cn/yanjiu/lunwen_68382.html
------分隔线----------------------------
推荐内容