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个人简介

招生专业: 院系名称 专业大类 一级学科 专业代码/专业名称 学位类型 招生类型 创新中药研究院 理学 中药学 100800/中药学 学术型 硕士 个人简历: 2017.06-目前 高级实验师,上海市中医药大学创新中药研究院手性药物研究中心 2013.01-2017.06 助理研究员,中国科学院上海有机化学研究所 2007.09-2012.12 博士,中国科学院上海有机化学研究所,导师:林国强研究员 2005.07-2006.06 实习研究员,珠海丽珠医药集团丽珠医药研究所 2001.09-2005.07 本科,武汉大学化学与分子科学学院 主持科研项目: 课题名称 项目名称 起止时间 金额 基于烯基结合环钯物种应用的串联双官能团化反应研究 上海市自然科学基金 2021.7-2024.06 50万

研究领域

不对称催化 有机合成

近期论文

查看导师最新文章 (温馨提示:请注意重名现象,建议点开原文通过作者单位确认)

[1] Xu Si-Yu, Zhang Rui, Zhang Shu-Sheng and Feng Chen-Guo. Enantioselective synthesis of 3-aryl-phthalides through a nickel- catalyzed stereoconvergent cross-coupling reaction[J]. Organic & Biomolecular Chemistry, 2021, . [2] Song Yi-Kang, Xu Si-Yu, Zhang Shu-Sheng, Fu Jian-Guo, Lin Guo-Qiang and Feng Chen-Guo. Palladium-Catalyzed Tandem γ-Arylation/Aromatization of Cyclohex-2-En-1-One Derivatives: A Route to 3,4-Dihydroanthracen-1(2H)-Ones[J]. Advanced Synthesis & Catalysis, 2021 . [3] 史传星 冯陈国, 陈雅丽, 张曙盛, 林国强. 苯并富烯合成方法研究进展[J]. 有机化学, 2020, 40(4): 817-830. [4] Zhang Shu-Sheng, Hu Tian-Jiao, Li Meng-Yao, Song Yi-Kang, Yang Xiao-Di, Feng Chen-Guo and Lin Guo-Qiang. Asymmetric Alkenylation of Enones and Imines Enabled by A Highly Efficient Aryl to Vinyl 1,4-Rhodium Migration[J]. Angewandte Chemie-International Edition, 2019, 58(11): 3387-3391. [5] Meng Jiao-Long, Jiao Tang-Qian, Chen Ya-Heng, Fu Rui, Zhang Shu-Sheng, Zhao Qian, Feng Chen-Guo and Lin Guo-Qiang. Synthesis of chiral isoindolinones via asymmetric propargylation/lactamization cascade[J]. Tetrahedron Letters, 2018, 59(16): 1564-1567. [6] Hu Hai-Jun, Zhou Yue, Han Zhu-Zhen, Shi Yan-Hong, Zhang Shu-Sheng, Wang Zheng-Tao and Yang Li. Abietane Diterpenoids from the Roots of Clerodendrum trichotomum and Their Nitric Oxide Inhibitory Activities[J]. Journal of Natural Products, 2018, 81(7): 1508-1516. [7] Yang Minghua, Zhang Shusheng, Zhang Xiang, Wang Haoyang, Zhang Fang, Hou Yuting, Su Yue and Guo Yinlong. An unexpected acid-catalyzed decomposition reaction of cilnidipine and pranidipine to the decarboxylative bridged tricyclic products via cascade rearrangements[J]. Organic Chemistry Frontiers, 2017, 4(11): 2163-2166. [8] Zhu Wei, Wang Hao-Yang, Zhang Junting, Zhang Shusheng and Guo Yinlong. Processed eggshell as sample carrier for rapid analysis of organometallic compounds by desorption electrospray ionization mass spectrometry[J]. Journal of Mass Spectrometry, 2015, 50(8): 972-977. [9] Zhu Hui, Zhang Shusheng, Wang Haoyang, Xu Bin and Guo Yinlong. Study on the Degradation of the Highly Reactive Hypervalent Trifluoromethylation Iodine Reagent PhI(OAc)(CF3)[J]. Chinese Journal of Chemistry, 2015, 33(12): 1365-1370. [10] Wang Hao-Yang, Zhang Jun-Ting, Zhang Shu-Sheng and Guo Yin-Long. The remarkable role of solvent in reaction mechanism studies by electrospray mass spectrometry[J]. Organic Chemistry Frontiers, 2015, 2(8): 990-994. [11] Wang Hao-Yang, Zhang Jun-Ting, Sun Shi-Hao, Zhang Shu-Sheng, Zhang Fang, Zhu Hui and Guo Yin-Long. Study on the accelerated Gutknecht selfcyclocondensation of amino-sugars under atmospheric pressure chemical ionization conditions[J]. Rsc Advances, 2015, 5(127): 105079-105083. [12] Zhang Shu-Sheng, Zhao Yi-Shuang, Tian Ping and Lin Guo-Qiang. Chiral NHC/Cu(I)-Catalyzed Asymmetric Hydroboration of Aldimines: Enantioselective Synthesis of alpha-Amido Boronic Esters[J]. Synlett, 2013, 24(4): 437-442. [13] He Xiaoshuang, Zhang Shusheng, Guo Yinlong, Wang Haoyang and Lin Guoqiang. Mechanistic Investigations of a Palladium-Diene Catalyzed Suzuki-Miyaura Cross-Coupling Reaction[J]. Organometallics, 2012, 31(8): 2945-2948. [14] Zhang Shu-Sheng, Wang Zhi-Qian, Xu Ming-Hua and Lin Guo-Qiang. Chiral Diene as the Ligand for the Synthesis of Axially Chiral Compounds via Palladium-Catalyzed Suzuki-Miyaura Coupling Reaction[J]. Organic Letters, 2010, 12(23): 5546-5549. [15] Wang Zhi-Qian, Feng Chen-Guo, Zhang Shu-Sheng, Xu Ming-Hua and Lin Guo-Qiang. Rhodium-Catalyzed Asymmetric Conjugate Addition of Organoboronic Acids to Nitroalkenes Using Chiral Bicyclo 3.3.0 Diene Ligands[J]. Angewandte Chemie-International Edition, 2010, 49(33): 5780-5783.

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