Zhenguang Zhao
Affiliations: | 2017-2022 | chemistry | Institute of Chemistry, The Hebrew University of Jerusalem |
Area:
peptide and protein chemistryGoogle:
"Zhenguang Zhao"Mean distance: (not calculated yet)
Parents
Sign in to add mentorJunfeng Zhao | grad student | 2014-2017 | Jiangxi Normal University | |
Norman Metanis | grad student | 2017-2021 | Hebrew University | |
Christina M. Woo | post-doc | 2022- | Harvard | |
(Postdoc.) |
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Publications
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Zhao Z, Laps S, Gichtin JS, et al. (2024) Selenium chemistry for spatio-selective peptide and protein functionalization. Nature Reviews. Chemistry |
Zhao Z, Mousa R, Metanis N. (2022) One-Pot Chemical Protein Synthesis Utilizing Fmoc-Masked Selenazolidine to Address the Redox Functionality of Human Selenoprotein F. Chemistry (Weinheim An Der Bergstrasse, Germany). e202200279 |
Zhao Z, Shimon D, Metanis N. (2021) Chemoselective Copper-Mediated Modification of Selenocysteines in Peptides and Proteins. Journal of the American Chemical Society |
Zhao Z. (2021) Chemoselective Copper-Mediated Modification of Selenocysteines in Peptides and Proteins J. Am. Chem. Soc.. 143: 12817-12824 |
Zhao Z, Metanis N. (2019) Utilizing copper-mediated deprotection of selenazolidine for cyclic peptides synthesis. The Journal of Organic Chemistry |
Zhao Z, Metanis N. (2019) Copper-mediated selenazolidine deprotection enables one-pot chemical synthesis of challenging proteins. Angewandte Chemie (International Ed. in English) |
Zhao Z, Peng Z, Zhao Y, et al. (2017) Hypervalent Iodine-Mediated Oxidative Rearrangement of N-H Ketimines: An Umpolung Approach to Amides. The Journal of Organic Chemistry |
Hu L, Xu S, Zhao Z, et al. (2016) Ynamides as racemization-free coupling reagents for amide and peptide synthesis. Journal of the American Chemical Society |
Zhao Z, Wang T, Yuan L, et al. (2016) ChemInform Abstract: Oxidative Acylation of Sulfoximines with Methylarenes as an Acyl Donor. Cheminform. 47: no-no |
Zhao Z, Wang T, Yuan L, et al. (2015) Oxidative acylation of sulfoximines with methylarenes as an acyl donor Rsc Advances. 5: 75386-75389 |