
姓名:王洪亮
硕士生导师
职称:副教授
联系方式:13220585201邮箱:hliang_18@sdfmu.edu.cn
研究方向:
1.有机化学反应机制研究
2.计算机辅助手性药物分子设计
主要学术任职:
担任J. Phys. Chem. A,J. Org. Chem.,Catal. Sci. Technol.等杂志审稿人
主要获奖情况(包括作为指导教师):
2023年,荣获山东省泰山学者(青年专家)称号
主持科研课题:
1.国家自然科学基金青年项目,22203051,钴催化不饱和烃硼氢化反应机理和选择性的理论研究,2023/01-2025/12,30万元,在研,主持
2.山东省自然科学基金青年项目,ZR2021QB047,钴催化不饱和烃硼氢化反应机理的理论研究,2022/01-2024/12,15万元,在研,主持
3.第69批中国博士后科学基金资助面上项目,2021M691917,2021/05-2022/10,8万元,结题,主持
4.第65批中国博士后科学基金资助面上项目,2019M652056,2019/05-2020/12,8万元,结题,主持
5.国家自然科学基金重大研究计划(培育项目),92156008,氮、磷、硅等杂原子手性中心的不对称氧化构筑,2022/01-2024/12,70万元,在研,主要参与人
6.国家自然科学基金面上项目,21773139,木质素模型化合物在酸性咪唑离子液体中溶解和降,2018/01-2021/12,65万元,结题,主要参与人
近五年代表性论文(限第一作者和通讯作者):
1.Peng Lu#;Hongliang Wang#,Yihui Mao,Xin Hong*, Zhan Lu*,Cobalt-Catalyzed Enantioconvergent Hydrogenation of Minimally Functionalized Isomeric Olefins,J. Am. Chem. Soc.2022,144(38):17359–17364.
2.Chenhui Chen#,Hongliang Wang#, Tongtong Li#, Dongpo Lu, Jiajing Li, Xie Zhang, Xin Hong*, and Zhan Lu*,Cobalt-Catalyzed Asymmetric Sequential Hydroboration/Isomerization/Hydroboration of 2-Aryl Vinylcyclopropanes,Angew. Chem. Int. Ed.2022,61: e202205619.
3.Jun Guo#,Hongliang Wang#,Shipei Xing,Xin Hong*, Zhan Lu*,Cobalt-Catalyzed Asymmetric Synthesis ofgem-Bis(silyl)alkanes by Double Hydrosilylation of Aliphatic Terminal Alkynes,Chem,2019,5(4):881–891.
4.Bo Zhou#,Hongliang Wang#, Zhong-Yan Cao, Jia-Wen Zhu, Ren-Xiao Liang, Xin Hong*, Yi-Xia Jia*,Dearomative 1,4-Difunctionalization of Naphthalenes via Palladium-Catalyzed Tandem Heck/Suzuki Coupling Reaction,Nat. Commun.,2020, 11: 4380.
5.Yuezhou Liu#,Hongliang Wang#,Liqing Shangguan, Peiren Liu, Bingbing Shi,*Xin Hong* and Feihe Huang* Selective Separation of Phenanthrene from Aromatic Isomer Mixtures by a Water-Soluble Azobenzene-Based Macrocycle,J. Am. Chem. Soc.2021,143(8): 3081–3085.
6.Yuezhou Liu#,Hongliang Wang#, Peiren Liu, Huangtianzhi Zhu, Bingbing Shi*, Xin Hong* and Feihe Huang* Azobenzene-Based Macrocyclic Arenes: Synthesis, Crystal Structures and Light-Controlled Molecular Encapsulation and Release,Angew. Chem. Int. Ed.2021, 60(11): 5766−5770.
7.Hongliang Wang, Shuo-Qing Zhang*, Xin Hong*,Computational studies on Ni-catalyzed amide C–N bond activation,Chem. Commun.,2019,55(76): 11330−11341.
8.Hongliang Wang, Mengmeng Dong, Chengbu Liu, Dongju Zhang*,Theoretical insight into the Zinc(II)-catalyzed synthesis of 2-indolyltetrahydroquinolines fromN-propargylanilines and indoles: a cross-dehydrogenative coupling with temporally separated catalytic activity,Catal. Sci. Technol.,2018, 8(7): 1997−2007.
9.Hongliang Wang, Chengbu Liu, Dongju Zhang*, Decisive effects of solvent and substituent on the reactivity of Ru-catalyzed hydrogenation of ethyl benzoate to benzyl alcohol and ethanol: a DFT study,Mol. Catal.,2017,440:120−132.
10.Yasheng Zhu#,Hongliang Wang#,Gang Wang, Zehua Wang, Zhaopeng Liu*, Lei Liu*, Enantioselective Construction of Single and Vicinal All-Carbon Quaternary Stereocenters through Ion-Pair-Catalyzed 1,6-Conjugate Addition,Org. Lett.2021,23(18):7248−7253.
11.Peiren Liu#,Hongliang Wang#, Hong Zeng, Xin Hong*, Feihe Huang*,A [15]paracyclophenone and its fluorenone-containing derivatives: syntheses and binding to nerve agent mimics via aryl-CH hydrogen bonding interactions,Org. Chem. Front.,2021,8(1):25−31.
12.Chenhui Chen#,Hongliang Wang#, Yufeng Sun, Jiayan Cui, Jianbo Xie, Yang Shi, Shijia Yu, Xin Hong*, Zhan Lu*, Iron-Catalyzed Asymmetric Hydrosilylation of Vinylcyclopropanes via Stereospecific C-C Bond Cleavage,iScience,2020,23(4):100985.
13.Hongliang Wang, Chengbu Liu, Dongju Zhang*,Mechanistic study on the Rh(III)-catalyzed synthesis of indolines via selective O-atom transfer of arylnitrones: origins of the regioselectivity and the improved yield with pivalic acid additive,J. Organomet. Chem.,2018,854: 15−26.
格式1.Liming Tan#, Kelvin Xi Zhang#, Matthew Y. Pecot, Sonal Nagarkar-Jaiswal, Pei-Tseng Lee, Shin-ya Takemura, Jason M. McEwen, Aljoscha Nern, Shuwa Xu, Wael Tadros, Zhenqing Chen, Kai Zinn, Hugo J. Bellen, Marta Morey*, S. Lawrence Zipursky*, Ig Superfamily Ligand and Receptor Pairs Expressed in Synaptic Partners in Drosophila, Cell, 2015, 163(7):
5−26.