Dawen Niu
Affiliations: | Sichuan University, Chengdu Shi, Sichuan Sheng, China |
Website:
http://www.theniugroup.com/index.phpGoogle:
"Dawen Niu"Bio:
https://scholar.google.com/citations?user=gTknK3UAAAAJ&hl=en
https://www.linkedin.com/pub/dawen-niu/34/5/9b6
Mean distance: 7.02
Parents
Sign in to add mentor| Thomas Robert Hoye | grad student | 2008-2013 | UMN | |
| (Total Synthesis of Okilactomycin D and Hexadehydro-Diels-Alder Reaction) | ||||
| Stephen L. Buchwald | post-doc | 2014- | MIT | |
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Publications
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| Niu D, Wang JX, Yao Y, et al. (2025) Cobalt-Catalyzed Hydroglycosylation of Alkynes for the Synthesis of Vinyl α-C-Glycosides. Angewandte Chemie (International Ed. in English). e202423631 |
| Wang JX, Chen MQ, Zhang Y, et al. (2024) A Modified Arbuzov-Michalis Reaction for Selective Alkylation of Nucleophiles. Angewandte Chemie (International Ed. in English). e202409931 |
| Li Y, Tian Y, Xie D, et al. (2024) Stereoselective synthesis of α-glycosyl azides: allyl glycosyl sulfones as radical precursors. Chemical Communications (Cambridge, England) |
| Liu D, Zhang Y, Niu D. (2024) Preparing glycosyl benzothiazoles from 2-isocyanoaryl thioethers and glycosyl radicals under thermal conditions. Chemical Communications (Cambridge, England) |
| Shang W, Niu D. (2023) Radical Pathway Glycosylation Empowered by Bench-Stable Glycosyl Donors. Accounts of Chemical Research |
| Zuo H, Zhang C, Zhang Y, et al. (2023) Base-Promoted Glycosylation Allows Protecting Group-Free and Stereoselective O-Glycosylation of Carboxylic Acids. Angewandte Chemie (International Ed. in English). e202309887 |
| Xu S, Zhang W, Li C, et al. (2023) Generation and Use of Glycosyl Radicals under Acidic Conditions: Glycosyl Sulfinates as Precursors. Angewandte Chemie (International Ed. in English) |
| Xie D, Wang Y, Zhang X, et al. (2022) Alkyl Sulfoxides as Radical Precursors and Their Use in the Synthesis of Pyridine Derivatives. Angewandte Chemie (International Ed. in English) |
| Sun HL, Wu B, Liu DQ, et al. (2022) Synthesis of Polydiynes an Unexpected Dimerization/Polymerization Sequence of C3 Propargylic Electrophiles. Journal of the American Chemical Society |
| Pu X, Dang QD, Yang L, et al. (2022) Doubly stereoconvergent construction of vicinal all-carbon quaternary and tertiary stereocenters by Cu/Mg-catalyzed propargylic substitution. Nature Communications. 13: 2457 |