硕士生导师、教授名单

黄海

发布时间:2021-01-07浏览次数:4746

黄海 教授

E-mail: huanghai@cczu.edu.cn

课题组网页:https://www.x-mol.com/groups/huanghaicczu


教育经历

2016.02-2017.01    美国内华达大学拉斯维加斯分校,博士联合培养,导师: Prof. Jun Yong Kang

2011.09-2016.12    南京工业大学,博士学位,导师: 朱红军 教授

2007.09-2011.07    南京工业大学,学士学位


工作经历

2020.01-至今         常州大学,教授

2019.05-2019.12      常州大学,一类雇员(香港科技大学博士后身份)

2018.07-2019.12      香港科技大学,博士后,合作导师: Prof. Jianwei Sun

2017.02-2018.04      美国内华达大学拉斯维加斯分校,博士后,合作导师: Prof. Jun Yong Kang.


承担项目

国家自然科学基金青年基金(22201023),30万,2023-2025

企业技术开发项目,60万,2022-2024

江苏省中以产业技术研究院开放课题(JSIITRI202205),3万,2022

江苏省双创人才(JSSCRC2021536),50万,2021-2024.

江苏省自然科学青年基金(BK20210849),20万,2021-2024.

国家自然基金重大研究计划-培育项目(91956114),37.5万,2020-2022.

江苏省高等学校自然科学研究面上项目20KJB1500125万,2020-2022.

常州市应用基础研究计划(CJ20200082),5万,2020-2022.

国家博士后基金-B类资助(2018M642226),5万,2018-2019.

江苏省博士后基金-A类资助(2018K027A),8万,2018-2019.


获奖情况

2020年度 ACS 个人贡献奖

2020年度 常州市十大青年科技新锐

2021年度 常州市第十六次自然科学优秀论文一等奖

科研方向

有机合成方法学:炔烃导向性官能团化,不对称催化,光催化等

论文发表

2022

34. Hongling Xie, Zhenkun Yang, Luning Tang, Zhengyu Han,* Jianwei Sun,* and Hai Huang.* Construction of Nine-memberedN,N,O-Heterocycles via Pdcatalyzed [6+3] Dipolar Cycloaddition.Chem. Commun.,2022,58, 10560-10563.

33. Zhengyu Han,Han Zhuang,Luning Tang,Yu Zang,Wengang Guo,Hai Huang,*and Jianwei Sun.*Catalytic Asymmetric Allylic Substitution/Isomerization with CentralChiralityTransposition.Org. Lett.,2022,24, 4246-4251.

32. Zhengyu Han, Yu Zang, Chang Liu, Wengang Guo, Hai Huang,* and Jianwei Sun.*Enantioselective Synthesis of Triarylmethanes via Organocatalytic Transfer Hydrogenation of para-Quinone Methides.Chem. Commun.,2022,58, 7128-7131.

31. Luning Tang, Yu Zang, Wengang Guo, Zhengyu Han, Hai Huang,*and Jianwei Sun.*Reductive Opening of Oxetanes Catalyzed by Frustrated Lewis Pairs:Unexpected Aryl Migration via Neighboring Group Participation.Org. Lett.2022,24, 3259-3264.

30. Danfeng Wang, Hai Huang*, Xiaolin Zhu*. Development of Anthrazoline Photocatalyst for Promoting Amination and Amidation Reactions. Chem. Commun. 2022, 58, 3529-3532.

29. Tianyu Zhang, Han Zhuang, Luning Tang, Zhengyu Han, Wengang Guo, Hai Huang,* and Jianwei Sun*. Catalytic Enantioselective Synthesis of 2,3-Dihydrobenzo[b]oxepines via Asymmetric Oxetane Opening by Internal Carbon Nucleophiles. Org. Lett.2022, 24, 207-212.

2021

28.Hai Huang, Jun Yong Kang*. Triflic Anhydride (Tf2O)-Activated Transformation of Amides, Sulfoxides and Phosphorus Oxides via Nucleophilic Trapping. Synthesis.2021, 54, 1157-1202.

27. Tianyu Zhang, Zhenkun Yang, Dapeng Zhou, Fuliang Meng, Zhengyu Han*, Hai Huang*.Non-metal Lewis acid-catalyzed cross-Claisen condensation for β-keto esters. Org. Biomol. Chem. 2021, 19, 9163-9166.

26. Shuxuan Liu, Hui Qian, Tianyu Zhang, Hongling Xie, Zhengyu Han, Wengang Guo, Hai Huang,* and Jianwei Sun*.Mild Intermolecular Synthesis of a Cyclopropane-Containing Tricyclic Skeleton: Unusual Reactivity of Isobenzopyryliums. Angew. Chem. Int. Ed.2021, 60, 21272-21276.

25. Wengang Guo, Min Wang, Zhengyu Han, Hai Huang* and Jianwei Sun*. Organocatalytic asymmetric synthesis of a-amino esters from sulfoxonium ylides. Chem. Sci., 2021, 12, 11191-11196.

24. Song Sun, Zhaobin Wang, Shijia Li, Cong Zhou, Lijuan Song, Hai Huang,* and Jianwei Sun*. An Organocatalytic Kinetic Resolution of Aziridines by Thiol Nucleophiles. Org. Lett.2021, 23, 554-558.

23. Hai Huang, Tianyu Zhang, and Jianwei Sun*. Mild C–C Bond Formation via Lewis Acid Catalyzed Oxetane Ring Opening with Soft Carbon Nucleophiles. Angew. Chem. Int. Ed. 2021, 60, 2668-2673.Highlighted by CBG.

2020

22. Shuxuan Liu, Yu Zang, Hai Huang*, and Jianwei Sun*. In(OTf)3-Catalyzed Synthesis of 2,3-Dihydro-1H-benzo[e]indoles and 2,3-Dihydrobenzofurans via [3 + 2] Annulation. Org. Lett. 2020, 22, 8219-8223.

21. Guannan Wang#, Hai Huang#, Wengang Guo, Chenxiao Qian, Jianwei Sun,*Unusual Skeletal Reorganization of Oxetanes for the Synthesis of 1,2-Dihydroquinolines.Angew. Chem. Int. Ed. 2020, 59,11245-11249.(# Co-first author)Highlighted by Synfacts.

2019

20. Hai Huang, Wen Yang, Zuliang Chen, Zengwei Lai, Jianwei Sun,* A mild catalytic synthesis of 2-oxazolines via oxetane ring-opening: rapid access to a diverse family of natural products. Chem. Sci., 2019, 10, 9586-9590.

入职常州大学前

19. Hai Huang, Johanna Denne, Chou-Hsun Yang, Haobin Wang, Jun Yong Kang.* Direct Aryloxylation/Alkyloxylation of Dialkyl Phosphonates for the Synthesis of Mixed Phosphonates [J]. Angew. Chem. Int. Ed. 2018, 57, 6624-6628. (Highlighted by UNLV news; Highlighted by Synpacts)

18. Hai Huang, Jun Yong Kang.* New Strategies for Activation of Phosphonates/Phosphates toForge Functional Phosphorus Compounds [J]. Synlett, 2019, 30, 635-641.

17. Hai Huang, Jeffrey Ash, Jun Yong Kang.* Tf2OPromoted Activating Strategy of Phosphate Analogues: Synthesis of Mixed Phosphates and Phosphinate [J]. Org. Lett.2018, 20, 4938-4941. (Highlighted by Organic Chemistry Portal).

16. Hai Huang, Jeffrey Ash, Jun Yong Kang.*Base-Controlled Fe(Pc)-Catalyzed Aerobic Oxidation of Thiols for the Synthesis of S-S and S-P(O) Bond [J]. Org. Biomol. Chem.2018, 16, 4236-4242.

15. Hai Huang, Hongjun Zhu, Jun Yong Kang.* Regio- and Stereoselective Hydrophosphorylation of Ynamides for the Synthesis of β-Aminovinylphosphine Oxides [J]. Org. Lett.2018, 20, 2778-2781.

14. Manasa Shetty,# Hai Huang,# Jun Yong Kang.* Regioselective Synthesis of α- and γ-Amino Quinolinyl Phosphonamides using N-Heterocyclic Phosphines (NHPs) [J]. Org. Lett.2018, 20, 700-703. (# Co-first author)

13. Hai Huang, Jun Yong Kang.* Organocatalytic Phosphonylation of in Situ Formed o Quinone Methides [J]. Org. Lett. 2017, 19, 5988-5991.

12. Hai Huang, Jun Yong Kang.* Oxidation-Reduction Condensation of Diazaphosphites for Carbon-Heteroatom Bond Formation Based on Mitsunobu Mechanism [J]. Org. Lett. 2017, 19, 544-547.

11. Luning Tang,# Hai Huang,# Yang Xi, Guangke He, Hongjun Zhu.* Pd/Cu-Catalyzed Tandem Head-to-tail Dimerization/Cycloisomerization of Terminal Ynamides for the Synthesis of 5-Vinyloxazolones [J]. Org. Biomol. Chem.2017, 15, 2923-2930 (# Co-first author)

10. Hai Huang, Jun Yong Kang.* Mitsunobu Reaction Using Basic Amines as Pronucleophiles [J]. J. Org. Chem. 2017, 82, 6604-6614. (Most Read Articles in JOC, 2017; Highlighted in Synfacts, 2017, 13, 807)

9. Hai Huang, Jake Palmas, Jun Yong Kang.* A Reagent-Controlled Phospha Michael Addition Reaction of Nitroalkenes with Bifunctional N-Heterocyclic Phosphine (NHP) Thioureas [J]. J. Org. Chem. 2016, 81, 11932-11939.

8. Hai Huang, Luning Tang, Xiaobo Han, Guangke He, Yang Xi, Hongjun Zhu.* Regioselective Iodoamination of Terminal Ynamides for the Synthesis of α-amino-β,β-diiodo-enamides [J]. Chem. Commun., 2016, 52, 4321-4324.

7. Hai Huang, Luning Tang, Qi Liu, Yang Xi, Guangke He,* Hongjun Zhu.* Formation of α-Chalcogenyl Acrylamides through Unprecedented Chalcogen Mediated Metal-Free Oxyfunctionalization of Ynamides with DMSO as Oxidant. Chem. Commun., 2016, 52, 5605-5608.

6. Hai Huang, Jun Yong Kang.* Amine-Catalyzed Phospha-Michael Reaction of α, β-Unsaturated Aldehydes and Ketones with Multifunctional N-Heterocyclic Phosphine-Thioureas as Phosphonylation Reagent. Org. Lett., 2016, 18, 4372-4375.

5. Hai Huang, Junzhen Fan, Guangke He,* Zhimin Yang, Xiaodong Jin, Qi Liu, Hongjun Zhu.* Generation of Oxazolidine-2,4-diones Bearing Thio-Quaternary Carbons by Oxothiolation / Cyclization of Ynamides. Chem. Eur. J., 2016, 22, 2532-2538.

4. Hai Huang, Luning Tang, Yang Xi, Guangke He, Hongjun Zhu.* Metal-free Hydration of Ynamides: Convenient Approach to Amides. Tetrahedron Lett.,2016, 57, 1873-1876.

3. Hai Huang, Guangke He, Guohao Zhu, Xiaolin Zhu, Shineng Qiu, Hongjun Zhu.* Palladium-Catalyzed Intramolecular Cyclization of Ynamides: Synthesis of 4-Halo-oxazolones. J. Org. Chem., 2015, 80, 3480-3487.

2. Hai Huang, Xiaolin Zhu, Guangke He, Qi Liu, Junzhen Fan, Hongjun Zhu.* Controlled Synthesis of 1,3,5-Oxadiazin-2-ones and Oxazolones through Regioselective Iodocyclization of Ynamides. Org. Lett., 2015, 17, 2510-2513.

1. Hai Huang, Guangke He, Xiaolin Zhu, Xiaodong Jin, Shineng Qiu, Hongjun Zhu.* Iodine-Mediated Oxidation of Ynamides: A Facile Access to N-Monosubstituted α-Ketoamides and α-Ketoimides. Eur. J. Org. Chem., 2014, 7174-7183.



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