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| 1 | Polyimides from 3, 3' - Dioxo - - spirodiphthalan - 5,5', 6, 6' -tetracarboxylic Dianhydride显示文摘 | Fushe Han Mengxian Ding Lianxun Gao | 1999 | Polymer1999，40，： | 1 |
| 2 | Fault Section Estimation in Power Systems Using a Genetic Algorithm 显示文摘 | WEN Fush uan HAN Zhe nxiang | 1995 | Electric Power Systems Research1995，34，： | 1 |
| 3 | 显示文摘 | Han Fushe Ding Mengxian Gao Lianxun | 1999 | Polymer1999，40，： | 1 |
| 4 | Preparation, characterization, and electrochromic properties of novel Co ( Ⅱ)-bis -2,2' :6' ,2' -terpyridine metallo -supramolecular polymers显示文摘 | Han Fushe HIGUCHI M AKASAKA Y | 2008 | Thin Solid Films2008，516，9： | 1 |
| 5 | CuCl2/8-Hydroxyquinoline-catalyzed α-Arylation of Diethyl Malonate with Aryl Bromides显示文摘 | YANG Jiuquan WU Guojie HE Yupeng HAN Fushe | 2018 | Chemical Research in Chinese Universities2018，34，5： | 0 |
| 6 | Design and Synthesis of Macrocyclic Polyoxazoles显示文摘 | QI Fuling GAO Lianxun HAN Fushe | 2014 | Chemical Research in Chinese Universities2014，30，4： | 0 |
| 7 | Design and Synthesis of Polyoxazole-based Macrocycles Tethered with a Phosphonate Group显示文摘We present the design and synthesis of polyoxazole-based macrocycles containing a phosphonate group.A reliable route was established that allows for convenient and versatile incorporation of various phosphonate functionalities such as phosphonate ester,acid,and salt at the macrocyclic ring periphery.Such unprecedented macrocyclic compounds are anticipated to be appealing candidates as telomerase inhibitors. | Fuling Qi Lianxun Gao Fushe Han | 2014 | Chinese Journal of Chemistry2014，32，7： | 0 |
| 8 | Cu2O-Mediated Room Temperature Cyanation of Aryl Boronic Acids/Esters and TMSCN显示文摘为经由芳基 boronic 酸或酉旨和 TMSCN 的 Cu2O-catalyed 跨 coupling 的芳基 nitriles 的有效、可靠的合成的一个方法被介绍。大量底层装饰了由充满电子、缺乏,位地,很拥挤、易变的功能被容忍。而且,反应能在房间温度在温和条件下面继续。作为催化剂与便宜、容易地可得到、没有卤素的 Cu2O 的使用配对的这些优点为芳基 cyanations 使协议成为一种呼吁的选择。 | Yong Ye Yanhua Wang Pengtang Liu Fushe Han | 2013 | Chinese Journal of Chemistry2013，31，1： | 0 |
| 9 | Synthesis of P-Stereogenic Diaryiphosphinamides as Novel Inhibitors of Melanoma显示文摘In this paper, the evaluation on the biological activity of an array of P-stereogenic diaryphosphinamides as novel inhibitors of malignant melanoma was presented. Among 20 derivatives being screened, several of them displayed high inhibition rate up to 90% against the B16 melanoma cells at 100 μg/mL. Moreover, one of them displayed high inhibition activity with IC50 value of 5.8 μg/mL. In contrast, a comparative assay showed that all the compounds were almost inactive or showed only very weak inhibition ability against an array of cell lines including HL7702, Bel7402, HT1080, A549 and McF7 cells. The results suggested that the P-stereogenic diaryiphosphinamides may serve as a class of novel lead molecules for further development of new inhibitors for selective inhibition of melanoma. | TANG Xu DU Zhijun WU Guojie HAN Fushe | 2019 | Chemical Research in Chinese Universities2019，35，5： | 0 |
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