[1] 刘玮炜, 赵跃强, 王钦琪, 李娜, 唐丽娟, 曾艳霞, LIU, Wei-Wei, ZHAO, Yue-Qiang, WANG, Qin-Qi, LI, Na, TANG, Li-Juan, ZENG, Yan-Xia. N-(4-苯基-噻唑-2-基)芳醛腙类化合物的合成 [J]. 有机化学 2008. [2] Min Wang, Liu-Fang Wang, Yi-Zhi Li, Qin-Xi Li, Zhi-Dong Xu, Dong-Ming Qu. Antitumour activity of transition metal complexes with the thiosemicarbazone derived from 3-acetylumbelliferone [J]. Transition Metal Chemistry 2001, 3(3). [3] TSUJI K, ISHIKAWA H. Synthesis and anti-pseudomonal activity of new 2-isocephems with a dihydroxypyridone moiety at C-7 [J]. Bioorganic and Medicinal Chemistry Letters 1994, 4. [4] Wilson KJ, Illig CR, Subasinghe N, Hoffman JB, Rudolph MJ, Soll R, Molloy CJ, Bone R, Green D, Randall T, Zhang M, Lewandowski FA, Zhou Z, Sharp C, Maguire D, Grasberger B, DesJarlais RL, Spurlino J. Synthesis of thiophene-2-carboxamidines containing 2-aminothiazoles and their biological evaluation as urokinase inhibitors. [J]. Bioorganic and Medicinal Chemistry Letters 2001, 7(7). [5] HAVIV F, RATAJCZYK J D, DENET RW. 3-[1-(2-Benzoxazolyl)hydrazino]propanenitrile derivatives:inhibitors of immune complex induced inflammation [J]. Journal of Medicinal Chemistry 1998, 31. [6] PATT W C, HAMILTON H W, TAYLOR M D. Structure-activity relationships of a series of 2-amino-4-thiazolecontaining renin inhibitors [J]. Journal of Medicinal Chemistry 1992, 35. [7] BELL F W, CANTRELL A S, HOEGBERG M. Phenethylthiazolethiourea (PETT) compounds, a new class of HIV-1 reverse transcriptase inhibitors.1.synthesis and basic structure-activity relationship studies of PETT analogs [J]. Journal of Medicinal Chemistry 1995, 38. [8] Gu XH, Wan XZ, Jiang B. Syntheses and biological activities of bis(3-indolyl)thiazoles, analogues of marine bis(indole)alkaloid nortopsentins. [J]. Bioorganic and Medicinal Chemistry Letters 1999, 4(4). [9] Jiang B, Gu XH. Syntheses and cytotoxicity evaluation of bis(indolyl)thiazole, bis(indolyl)pyrazinone and bis(indolyl)pyrazine: analogues of cytotoxic marine bis(indole) alkaloid. [J]. Bioorganic and medicinal chemistry 2000, 2(2). [10] KUMAR Y, GREEN R, BORYSKO K Z. Synthesis of 2, 4-disubstituted thiazoles and selenazoles as potential antitumor and antifilarial agents:1.Methyl 4-(isothiocyanatomethyl)thiazole-2-carbamates, -selenazole-2-carbamates, and related derivatives [J]. Journal of Medicinal Chemistry 1993, 36. [11] KUMAR Y, GREEN R, WISE D S. Synthesis of 2, 4-disubstituted thiazoles and selenazoles as potential antifilarial and antitumor agents:2.2-Arylamido and 2-alkylamido derivatives of 2-amino-4-(isothiocyanatomethyl)thiazole and 2-amino-4-(isothiocyanatomethyl)selenazole [J]. Journal of Medicinal Chemistry 1993, 36. [12] Chimenti F, Bizzarri B, Maccioni E, Secci D, Bolasco A, Chimenti P, Fioravanti R, Granese A, Carradori S, Tosi F. A Novel Histone Acetyltransferase Inhibitor Modulating Gcn5 Network: Cyclopentylidene-[4-(4 '-chlorophenyl)thiazol-2-yl)hydrazone [J]. Journal of Medicinal Chemistry 2009, 2(2). [13] KAMBLE V T, DAVANE B S, CHAVAN S A. An efficient and green procedure for the preparation of 2-{2-[N-(2-hydroxybemylidene) hydrazino]-thiazol-4-yl } phenols [J]. Australian Journal of Chemistry 2007, 60. [14] Zhang, D.-N., Li, J.-T., Song, Y.-L., Liu, H.-M., Li, H.-Y.. Efficient one-pot three-component synthesis of N-(4-arylthiazol-2-yl) hydrazones in water under ultrasound irradiation [J]. Ultrasonics sonochemistry 2012, 3(3). [15] Doris Dallinger, C.Oliver Kappe. Microwave-Assisted Synthesis in Water as Solvent [J]. Chemical Reviews 2007, 6(6). [16] KAPPE C O. Controlled microwave heating in modem organic synthesis [J]. Angewandte Chemie International Edition 2004, 43. |