De-Wei Gao
Affiliations: | 2018-2020 | Shanghai Institute of Organic Chemistry, PR China |
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Parents
Sign in to add mentorShu-li You | grad student | 2011-2016 | Shanghai Institute of Organic Chemistry |
Keary Mark Engle | post-doc | 2016-2018 | Scripps Institute |
Yi Tang | post-doc | 2018-2020 | UCLA |
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Publications
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Sun YW, Zhao JH, Yan XY, et al. (2024) Asymmetric synthesis of atropisomers featuring cyclobutane boronic esters facilitated by ring-strained B-ate complexes. Nature Communications. 15: 10810 |
Jiang XM, Ji CL, Ge JF, et al. (2023) Asymmetric Synthesis of Chiral 1,2-Bis(Boronic) Esters Featuring Acyclic, Non-Adjacent 1,3-Stereocenters. Angewandte Chemie (International Ed. in English). e202318441 |
Chen A, Qiao Y, Gao DW. (2023) Controllable Regiodivergent Alkynylation of 1,3-Bis(Boronic) Esters Activated by Distinct Organometallic Reagents. Angewandte Chemie (International Ed. in English). e202312605 |
Ge JF, Zou XZ, Liu XR, et al. (2023) Ir-Catalyzed Enantioselective Synthesis of gem-Diborylalkenes Enabled by 1,2-Boron Shift. Angewandte Chemie (International Ed. in English). e202307447 |
Gao DW, Jamieson CS, Wang G, et al. (2020) A Polyketide Cyclase That Forms Medium-Ring Lactones. Journal of the American Chemical Society |
Gao DW, Gao Y, Shao H, et al. (2020) Cascade CuH-Catalysed Conversion of Alkynes to Enantioenriched 1,1-Disubstituted Products. Nature Catalysis. 3: 23-29 |
Nimmagadda SK, Liu M, Karunananda MK, et al. (2019) Catalytic, Enantioselective α-Alkylation of Azlactones with Non-Conjugated Alkenes via Directed Nucleopalladation. Angewandte Chemie (International Ed. in English) |
Gao DW, Xiao Y, Liu M, et al. (2018) Catalytic, Enantioselective Synthesis of Allenyl Boronates. Acs Catalysis. 8: 3650-3654 |
Gao DW, Vinogradova EV, Nimmagadda SK, et al. (2018) Direct Access to Versatile Electrophiles via Catalytic Oxidative Cyanation of Alkenes. Journal of the American Chemical Society |
O'Duill ML, Matsuura R, Wang Y, et al. (2017) Tridentate Directing Groups Stabilize 6-Membered Palladacycles in Catalytic Alkene Hydrofunctionalization. Journal of the American Chemical Society |