Haoyuan Wang
Affiliations: | University of California, San Francisco, San Francisco, CA |
Area:
Organic Chemistry; Chemical Biology; Cancer BiologyGoogle:
"Haoyuan Wang"Mean distance: (not calculated yet)
Parents
Sign in to add mentor| Aiwen Lei | research assistant | 2009-2011 | Wuhan University | |
| Zhangjie Shi | research assistant | 2011-2012 | Peking University | |
| Weiping Tang | grad student | 2012-2017 | UW Madison | |
| (Development of Novel Glycosylation Reactions Using Transition Metals or Organocatalysts) | ||||
| Jack Taunton | post-doc | 2017- | UCSF | |
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Publications
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| Holm M, Natchiar SK, Rundlet EJ, et al. (2023) mRNA decoding in human is kinetically and structurally distinct from bacteria. Nature |
| Oltion K, Carelli JD, Yang T, et al. (2023) An E3 ligase network engages GCN1 to promote the degradation of translation factors on stalled ribosomes. Cell. 186: 346-362.e17 |
| Wang HY, Yang H, Holm M, et al. (2022) Synthesis and single-molecule imaging reveal stereospecific enhancement of binding kinetics by the antitumour eEF1A antagonist SR-A3. Nature Chemistry |
| Klein VG, Bray WM, Wang HY, et al. (2021) Identifying the Cellular Target of Cordyheptapeptide A and Synthetic Derivatives. Acs Chemical Biology |
| Gordon DE, Jang GM, Bouhaddou M, et al. (2020) A SARS-CoV-2 protein interaction map reveals targets for drug repurposing. Nature |
| Wen P, Simmons CJ, Ma ZX, et al. (2020) Synthesis of Glycosyl Chlorides and Bromides by Chelation Assisted Activation of Picolinic Esters under Mild Neutral Conditions. Organic Letters |
| Wang HY, Blaszczyk SA, Xiao G, et al. (2017) Chiral reagents in glycosylation and modification of carbohydrates. Chemical Society Reviews |
| Wang HY, Simmons CJ, Blaszczyk SA, et al. (2017) Isoquinoline-1-carboxylate as a Traceless Leaving Group for Chelation-Assisted Glycosylation under Mild Neutral Conditions. Angewandte Chemie (International Ed. in English) |
| Wang HY, Simmons CJ, Zhang Y, et al. (2017) Chiral Catalyst-Directed Dynamic Kinetic Diastereoselective Acylation of Anomeric Hydroxyl Groups and a Controlled Reduction of the Glycosyl Ester Products. Organic Letters |
| Zhu Z, Wang H, Simmons C, et al. (2017) Iridium-Catalyzed Dynamic Kinetic Stereoselective Allylic Etherification of Achmatowicz Rearrangement Products Advanced Synthesis & Catalysis. 360: 595-599 |