张曙盛

发布者:创新中药1发布时间:2021-04-25浏览次数:319

姓名:张曙盛性别:
职称:高级实验师学历:博士研究生
专家类别:
职务:
电话:021-51322672传真:
电子邮箱:zhangss@shutcm.edu.cn
通讯地址:上海市蔡伦路1200号 上海中医药大学 邮编:201203
个人主页:

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

研究内容:

不对称催化
有机合成

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 2021.7-2024.0650万

发表文章:

[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.