高得伟

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高得伟课题组介绍

课题组长  研究介绍   发表论文  本组成员

 




高得伟,助理教授、研究员、博士生导师

通讯地址:上海科技大学物质学院3号楼505-2

电子邮件:gaodw@shanghaitech.edu.cn 

ORCiD: 0000-0002-6258-8378

课题组网站https://www.x-mol.com/groups/dwgao

个人简历

2020年9-至今,上海科技大学物质科学与技术学院,助理教授,研究员,博士生导师

2018.11-2020.9,加州大学洛杉矶分校,博士后,导师:Prof. Yi Tang

2016.9-2018.10,美国斯克利普斯研究所,博士后,导师:Prof. Keary Mark Engle                                  

2011.9-2016.7,中国科学院上海有机化学研究所,博士,导师:游书力 院士

2007.9-2011.7,东北林业大学,学士,导师:彭进松 教授

Honor and Awards:

2024年Thieme Chemistry Journals Award

2021年上海市高层次引进人才

2020年青年东方学者

2016年上海市优秀毕业生

2016年度中科院-沙特基础工业公司奖学金

2015年度博士研究生国家奖学金

2015年NSFC-RSC International Symposium on Emerging Frontiers in Organic Chemistry (Outstanding Poster Prize)

2014年中科院院长奖学金

 

 

课题组侧重于发展新型催化剂以及催化新策略和新方法,拓展催化的反应类型,实现含硼有机化合物与功能分子的可控、高选择性合成。同时注重从原子/分子层次探索并理解反应的机理,为进一步拓展新型催化反应提供理论指导。具体主要从以下三个方向开展研究工作:

(1) 开发合成有机硼化物的不对称催化反应

(2) 发展基于有机硼和硅化合物的新型偶联反应

(3) 开展硼元素化学生物学的研究


1. 诚聘助理研究员(事业编制),申请人需有有机化学博士学位和博士后工作经验;

待遇优厚,享受优惠住房政策;学校为助理研究员本人和子女购买补充医疗保险;同时享受学校,工会,课题组等发放的各种福利与津贴。

2. 诚聘博士后,申请人需有有机化学博士学位.

条件优秀者可申请上科大双一流博士后项目,廉价租住上科大博士后公寓,享受学校,工会,课题组等发放的各种福利与津贴。

 

 


Independent Research

2024

(27) Zou, X.-Z.+; Ge, J.-F.+; Yang, Y.-X.; Huang, Y.-F.; Gao, D.-W.* Regioselective Alkynylation and Alkenylation at the More Hindered C–B Bond of 1,2-Bis(Boronic) Esters. Org. Lett202426, 1595 (published as part of Organic Letters virtual special issue Radical Reactions for the Construction and Transformation of Complex Molecules).

(26) Ji, C.-L.; Gao, D.-W.* Stereoselective Synthesis of 1,2-Bis(Boronates). Trends Chem. 2024, 6, 211.

(25) Ji, C.-L.; Gao, D.-W.* Recent Advances in Catalytic Asymmetric Synthesis of 1,2-Bis(Boronic) Esters. Chin. J. Org. Chem. 2024, 44, 10.6023/cjoc202312014 (Invited Review).

(24) Sun, Y.-W.; Gao, D.-W.* Asymmetric Synthesis of Organoborons via Ir-Catalyzed Stereoconvergent Reactions. Chem Catal. 2024, 4, 100896 (Invited Preview).

(23) Chen, A.; Ji, C.-L.Gao, D.-W.* Precision Alkynylation of 1,3-Bis(Boronates) Utilizing Distinct Organometallic Reagents for Regioselective Synthesis. Synlett 2024, 10.1055/a-2236-5948 (Invited Synpacts).

(22) Jiang, X.-M.; Ji, C.-L.; Ge, J.-F.; Zhao, J.-H.; Zhu, X.-Y.; Gao, D.-W.* Asymmetric Synthesis of Chiral 1,2-Bis(Boronic) Esters Featuring Acyclic, Non-Adjacent 1,3-Stereocenters. Angew. Chem. Int. Ed. 2024, 63, e202318441. (Highlighted in "Mechanism of the Month" of Trends in Chemistry)

2023

(21) Chen, A; Qiao, Y.; Gao, D.-W.* Controllable Regiodivergent Alkynylation of 1,3-Bis(Boronic) Esters Activated by Distinct Organometallic ReagentsAngew. Chem. Int. Ed202362, e202312605 (Selected as "VIP"; highlighted in Chin. J. Org. Chem. 2023, 43, 4311-4313.).

(20) Gao, D.-W. Angew. Chem. Int. Ed202362, e202309675 (Introducing...).

(19) Ge, J.-F.+; Zou, X.-Z.+; Liu, X.-R.+; Ji, C.-L.; Zhu, X.-Y.; Gao, D.-W.* Ir-Catalyzed Enantioselective Synthesis of gem-Diborylalkenes Enabled by 1,2-Boron Shift. Angew. Chem. Int. Ed2023, 62, e202307447.(Highlighted in Synfacts 2023, 19, 995)

2022

(18) Jiang, X.-M.; Liu, X.-R.; Chen, A.; Zou, X.-Z.; Ge, J.-F.; Gao. D.-W.* 1,2-Boryl Migration Enables Efficient Access to Versatile Functionalized Boronates. Eur. J. Org. Chem. 2022, e202101463. (Invited review for the #NextGenOrgChem special collection.)


Before joining ShanghaiTech University

(17) Gao, D.-W.; Jamieson, C. S.; Wang, G.; Yan, Y.; Zhou, J.; Houk, K. N.; Tang, Y. A Polyketide Cyclase That Forms Medium-Ring Lactones. J. Am. Chem. Soc. 2021, 143, 80–84. (Authors contributed equally)

(16) Gao, D.-W.; Gao, Y.; Shao, H.; Qiao, T.-Z.; Wang, X.; Sanchez, B.; Chen, J. S.; Liu, P.; Engle, K. M. Cascade CuH-Catalyzed Conversion of Alkynes to Enantioenriched 1,1-Disubstituted Products. Nat. Catal. 20203, 2329.(Authors contributed equally).

(15) Gao, D.-W.; Vinogradova, E. V.; Nimmagadda, S. K.; Medina, J. M.; Xiao, Y.; Suciu, R. M.; Cravatt, B. M.; Engle, K. M. Direct Access to Versatile Electrophiles via Catalytic Oxidative Cyanation of Alkenes. J. Am. Chem. Soc. 2018, 140, 80698073. (Top 1“Most Read Article”in June 2018.; Featured in Organic Chemistry Highlights.)

(14) Gao, D.-W.; Xiao, Y.; Liu, M.; Liu, Z.; Karunananda, M. K.; Chen, J. S.; Engle, K. M. Catalytic, Enantioselective Synthesis of Allenyl Boronates. ACS Catal. 2018, 8, 36503654. (Highlighted in the Jan/Feb ChemRxiv Round-up; Highlighted in Synfacts 2018, 14, 734.; Featured in Organic Chemistry Highlights on October 22, 2018.; One of the “Most Read Articles” in March 2018.)

(13) Gao, D.-W.; Gu, Q.; Zheng, C.; You, S.-L. Synthesis of Planar Chiral Ferrocenes via Transition-Metal-Catalyzed Direct C–H Bond Functionalization. Acc. Chem. Res. 2017, 50, 351–365.

(12) Gao, D.-W.; Gu, Y.; Wang, S.-B.; Gu, Q.; You, S.-L. Pd(0)-Catalyzed Asymmetric C–H Alkenylation for Efficient Synthesis of Planar Chiral Ferrocenes. Organometallics 2016, 35, 3227–3233.

(11) Gao, D.-W.; Gu, Q.; You, S.-L. An Enantioselective Oxidative CH/CH Cross-Coupling Reaction: Highly Efficient Method To Prepare Planar Chiral Ferrocenes. J. Am. Chem. Soc. 2016, 138, 2544–2547. (Highlighted by Chemical & Engineering News on March 14, 2016.)

(10) Gao, D.-W.; Zheng, C.; Gu, Q.; You, S.-L. Pd-Catalyzed Highly Enantioselective Synthesis of Planar Chiral Ferrocenylpyridine Derivatives. Organometallics 2015, 34, 4618–4625.

(9) Gao, D.-W.; Gu, Q.; You, S.-L. Pd(II)-Catalyzed Intermolecular Direct CH Bond Iodination: An Efficient Approach toward the Synthesis of Axially Chiral Compounds via Kinetic Resolution. ACS Catal2014, 4, 2741–2745. (One of the “Most Read Articles”in July 2014.; Highlighted in ACS Catal. Spotlights.)

(8) Gao, D.-W.; Yin, Q.; Gu, Q.; You, S.-L. Enantioselective Synthesis of Planar Chiral Ferrocenes via Pd(0)-Catalyzed Intramolecular Direct CH Bond Arylation. J. Am. Chem. Soc. 2014, 136, 4841–4844. (Highlighted by Synfacts 2014, 10, 597.)

(7) Gao, D.-W.; Shi, Y.-C.; Gu, Q.; Zhao, Z.-L.; You, S.-L. Enantioselective Synthesis of Planar Chiral Ferrocenes via Palladium-Catalyzed Direct Coupling with Arylboronic Acids. J. Am. Chem. Soc. 2013, 135, 86–89. (Highlighted by Synfacts 2013, 9, 0417.; Highlighted by Chin. J. Org. Chem. 2013, 33, 654.)

(6) Nimmagadda, S. K.; Liu, M.; Karunananda, M. K.; Gao, D.-W.; Apolinar, O.; Chen, J. S.; Liu, P.; Engle, K. M. Catalytic, Enantioselective α-Alkylation of Azlactones with Non-Conjugated Alkenes via Directed Nucleopalladation. Angew. Chem. Int. Ed. 2019, 58, 3923–3927.

(5) O’Duill, M. L.; Matsuura, R.; Wang, Y.; Turnbull, J. L.; Gurak Jr, J. A.; Gao, D.-W.; Lu, G.; Liu, P.; Engle, K. M. Tridentate Directing Groups Stabilize 6-Membered Palladacycles in Catalytic Alkene Hydrofunctionalization. J. Am. Chem. Soc. 2017, 139, 15576–15579.

(4) Wang, J.; Gao, D.-W.; Huang, J.; Tang, S.; Xiong, Z.; Hu, H.; You, S.-L.; Zhu, Q. Palladium-Catalyzed Enantioselective C(sp2)–H Imidoylation by Desymmetrization. ACS Catal. 2017, 7, 3832–3836.

(3) Yin, Q.; Wang, S.-G.; Liang, X.-W.; Gao, D.-W.; Zheng, J.; You, S.-L. Asymmetric Dearomative Chlorination of β-Naphthols. Chem. Sci. 2015, 6, 4179–4183.

(2) Shi, Y.-C.; Yang, R.-F.; Gao, D.-W.; You, S.-L. Enantioselective Synthesis of Planar Chiral Ferrocenes via Palladium-Catalyzed Annulations with Diarylethynes. Beilstein J. Org. Chem.2013, 9, 1891–1896.

(1) Peng, J.; Zong, C.; Ye, M.; Chen, T.; Gao, D.-W.; Wang, Y.; Chen, C. Direct Transition-Metal-Free Intramolecular C–O Bond Formation: Synthesis of Benzoxazole Derivatives. Org. Biomol. Chem. 2011, 9, 12251230.


   

       BOOK CHAPTER

(1) Gao, D.-W.; Zheng, J.; Ye. K.-Y.; Zheng. C.; You, S.-L. Asymmetric Functionalization of C–H Bonds via a Transient Carbon-Metal (C–M) Species. in Asymmetric Functionalization of C–H Bonds, You, S.-L., Ed., Royal Society of Chemistry 2015, pp.141-213.

 

PATENTS

(1) You, S.-L.; Gao, D.-W.; Gu, Q. A Kind of Planar Chiral Ferrocene Compounds, Synthetic Methods and Their Applications. The Number of Patent (ZL201510757648.8).

(2) You, S.-L.; Gao, D.-W.; Yin, Q.; Gu, Q. The Preparation of Planar Chiral Ferrocene Derivatives and Their Applications. The Number of Patent (ZL201410040306.X).

(3) You, S.-L.; Gu, Q.; Gao, D.-W.; Shi, Y.-C.; Zhao, Z.-L. The Synthesis of New Kind of Planar Chiral Ferrocene Compounds and Their Applications. The Number of  Patent (ZL201210489246.0).

 

 





 

 




 


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