Dewei Gao

Date:2020-10-10Views:2229设置

高得伟课题组介绍

Principal Investigator  Research  Publications  Team



Principal Investigator




 


De-Wei Gao (高得伟), Assistant Professor, PI

Address: School of Physical Science and Technology, ShanghaiTech University

Email: gaodw@shanghaitech.edu.cn

ORCiD: 0000-0002-6258-8378

Website: https://www.x-mol.com/groups/dwgao

Curriculum Vitae:

2020.9-current, ShanghaiTech University, Assistant Professor, PI

2018.11-2020.9, University of California, Los Angeles (UCLA), Postdoctoral Fellow, AdvisorProf. Yi Tang

2016.9-2018.10, The Scripps Research Institute (TSRI), Postdoctoral Fellow, AdvisorProf. Keary Mark Engle                                  

2011.9-2016.7, Shanghai Institute of Organic Chemistry (SIOC), Chinese Academy of Sciences, Ph.D., Advisor: Prof. Shu-Li You

2007.9-2011.7, Northeast Forestry University, B.S., Advisor: Prof. Jinsong Peng

Honor and Awards:

Science of Synthesis Early Career Advisory Board, 2025

Thieme Chemistry Journals Award, 2024

Shanghai Young Leading Talent, 2021

Shanghai Young Eastern Scholar, 2020

Shanghai Outstanding Graduate Student, 2016

SABIC (Saudi Basic Industries Corporation)-CAS (Chinese Academy of Sciences) Scholarship, 2016

National Scholarship for Excellent Ph.D. Students, 2015

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

CAS Presidential Scholarship (Excellent Prize), 2014


 


Research



 

Our group is extremely interested in the design of novel catalysts and new catalytic systems, achieving selective synthesis of highly valuable compounds. Additionally, our team intends to develop biocompatible reactions by using photocatalytic strategies.


Postdoctoral Scholars and Research Assistants are available immediately in the Gao group. Please send CV, research summary and list of two references to Prof. Gao by email (gaodw@shanghaitech.edu.cn).


 


Publications



 


Independent Research

2024

(30) Sun, Y.-W.+; Zhao, J.-H.+; Yan, X.-Y.; Ji, C.-L.; Feng, H.*; Gao, D.-W.* Asymmetric Synthesis of Atropisomers Featuring Cyclobutane Boronic Esters Facilitated by B-ate Complexes. Nat. Commun. 2024, 15, 10.1038/S41467-024-55161-6.

(29) Zhao, J.-H.+; Chen, A.+; Zou, X.-Z.+; Ji, C.-L.*; Feng, H.*; Gao, D.-W.* Catalytic Selective Functionalization of Poly(organoborons). Chin. J. Chem. 2024, 42, 3484-3498 (Invited review).

(28) 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, 1595-1600 (Featured in Org. Chem. Highlights; published as part of Organic Letters virtual special issue "Radical Reactions for the Construction and Transformation of Complex Molecules").

(27) Ji, C.-L.; Gao,  D.-W.* Stereoselective Synthesis of 1,2-Bis(Boronates). Trends Chem. 2024, 6, 211-212.

(26) Ji, C.-L.; Gao, D.-W.* Recent Advances in Catalytic Asymmetric Synthesis of 1,2-Bis(Boronic) Esters. Chin. J. Org. Chem. 2024, 44, 1385-1402 (Invited Review).

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

(24) Chen, A.+; Ji, C.-L.+; Gao, D.-W.* Precision Alkynylation of 1,3-Bis(Boronates) Utilizing Distinct Organometallic Reagents for Regioselective Synthesis. Synlett 2024, 35, 1839-1843 (Invited Synpacts, selected as the Cover of Synlett).

(23) 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

(22) 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.).

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

(20) 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

(19) 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. Chem2022, e202101463. (Invited review for the #NextGenOrgChem special collection.)


        Before joining ShanghaiTech University (Selected Publications)

(18) 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, 8084. (Authors contributed equally)

(17) 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).

(16) 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. Soc2018140, 80698073. (Top 1 “Most Read Article” in June 2018.; Featured in Organic Chemistry Highlights.)

(15) 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 Catal20188, 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.)

(14) 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.

(13) 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.

(12) 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. 2016138, 2544–2547. (Highlighted by Chemical & Engineering News on March 14, 2016.)

(11) 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.

(10) 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 Catal20144, 2741–2745. (One of the “Most Read Articles”in July 2014.; Highlighted in ACS Catal. Spotlights.)

(9) 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. 2014136, 4841–4844. (Highlighted by Synfacts 201410, 597.)

(8) 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. 2013135, 86–89. (Highlighted by Synfacts 20139, 0417.; Highlighted by Chin. J. Org. Chem201333, 654.)

(7) Song, Y.; Wang, W.; Yang, J.; Gao, D.-W.; Billingsley, J. M.; Wang, S.; Zhu, Y.; Wang, J.; Ju, J.;Yan, Y.; Tang, Y. Beta-Terrecyclene synthase constructs the quadrane backbone in terrecyclic acid biosynthesis. Chem. Sci. 2024, 15, 8750-8755.

(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. 201958, 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. 2017139, 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. 20177, 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. 20156, 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.20139, 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. Chem20119, 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).



 


Team








 

 




 

 


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