Zobrazeno 1 - 10 of 72 pro vyhledávání: '"Qin-Pei Wu"'
1
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Futuristic Variations and Analysis in Fundus Images Corresponding to Biological Traits
Autor: Hassan, Muhammad, Zhang, Hao, Ameen, Ahmed Fateh, Zeng, Home Wu, Ma, Shuye, Liang, Wen, Shang, Dingqi, Ding, Jiaming, Zhan, Ziheng, Lam, Tsz Kwan, Xu, Ming, Huang, Qiming, Wu, Dongmei, Zhang, Can Yang, You, Zhou, Ain, Awiwu, Qin, Pei Wu
Fundus image captures rear of an eye, and which has been studied for the diseases identification, classification, segmentation, generation, and biological traits association using handcrafted, conventional, and deep learning methods. In biological tr
Externí odkaz: http://arxiv.org/abs/2302.03839
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2
Determining Essential Requirements for Fluorophore Selection in Various Fluorescence Applications Taking Advantage of Diverse Structure–Fluorescence Information of Chromone Derivatives
Autor: Huaqing Cui, Yikun Chen, Gang Zhang, Hui Wen, Wang Yuchen, Yujun He, Yongxin Gao, Qin-Pei Wu
Publikováno v: Journal of Medicinal Chemistry. 64:1001-1017
Herein, we report our work exploring the essential requirements for fluorophore selection during the development of various fluorescence applications. We assembled a library of chromone-derived fluorophores with diverse structure-fluorescence propert
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::387a43a27c51a6f0865fc58fa50910fc
https://doi.org/10.1021/acs.jmedchem.0c01508
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5
Efficient Synthesis of 5-Trifluoromethylthio-1,2,3-Triazoles: One-Pot Multicomponent Reaction from Elemental Sulfur and TMSCF3
Autor: Qin-Pei Wu, Meng-Tian Li, Liang-Liang Shen, Lin-Lin Zhang
Publikováno v: Synthesis. 52:304-310
A sequential multistep reaction toward 5-trifluoromethyl­thio-1,2,3-triazoles has been established, starting from alkynes, organo­azides, S8, and (trifluoromethyl)trimethylsilane (TMSCF3). This reaction features mild conditions, easy operation, and
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ffde7be7196dd08165dd69798d9fb60b
https://doi.org/10.1055/s-0039-1690716
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6
Synthesis, Anti-Varicella-Zoster Virus and Anti-Cytomegalovirus Activity of 4,5-Disubstituted 1,2,3-(1H)-Triazoles
Autor: Dominique Schols, Bei Yang, Qin-Pei Wu, Ning-Ning Liu, Robert Snoeck, Yong-Wei Wu, Graciela Andrei, Zhuo-Yong Zhang, Yu-Hong Xiang, Xue Chen, Yi-ning Wen, Wei-yuan Yuan, Zhen Jiang
Publikováno v: Medicinal Chemistry. 15:801-812
Background: Clinical drugs for herpesvirus exhibit high toxicity and suffer from significant drug resistance. The development of new, effective, and safe anti-herpesvirus agents with different mechanisms of action is greatly required. Objective: Nove
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19a9eee3fbc19a258663753de9dba206
https://doi.org/10.2174/1573406414666181109095239
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7
Efficient Synthesis of Diverse 5-Thio- or 5-Selenotriazoles: One-Pot Multicomponent Reaction from Elemental Sulfur or Selenium
Autor: Zhi-Bin Xu, Ting Gao, Qi-Pu Dai, Bei Yang, Ya-Ting Li, Qin-Pei Wu, Sha-Sha Guo, Zi-Hui Meng, Lin-Lin Zhang
Publikováno v: Synthesis. 51:4170-4182
A sequential multistep reaction toward 5-thio- or 5-selenotriazoles has been established by generation of both copper(I) triazolides and sulfenylating or selenylating agents in situ, starting from elemental sulfur or selenium. This reaction features
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::220e370d4e173ee3f57d98db1bd86b32
https://doi.org/10.1055/s-0039-1690618
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9
A Mild Multi-Component Reaction for the Synthesis of 4,5-Disubstituted 1H-1,2,3-Triazoles from Phosphonium Salts, Aldehydes, and Sodium Azide
Autor: Qin-Pei Wu, Guang-Long Wu
Publikováno v: Synthesis. 50:2768-2774
A mild and metal-free multi-component reaction to synthesize 4,5-disubstituted 1H-1,2,3-triazoles from phosphonium salts, aldehydes, and sodium azide is described. The process undergoes an organocatalyzed coupling of formyl group with phosphonium to
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::bc1b897ecc9bce0ba2c8346755075722
https://doi.org/10.1055/s-0037-1609720
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