Pengpeng Zhang
Affiliations: | Zhejiang University, Hangzhou Shi, Zhejiang Sheng, China |
Area:
organic chemistry, MLGoogle:
"Pengpeng Zhang"Mean distance: (not calculated yet)
Parents
Sign in to add mentor| Zhen Yang | grad student | 2013-2018 | |
| Timothy R. Newhouse | post-doc | 2018-2023 |
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Publications
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| Cuomo AE, Ibarraran S, Sreekumar S, et al. (2023) Feed-Forward Neural Network for Predicting Enantioselectivity of the Asymmetric Negishi Reaction. Acs Central Science. 9: 1768-1774 |
| Zhang P, Newhouse TR. (2023) Palladium-Catalyzed Carbonylative Difunctionalization of Unactivated Alkenes Initiated by Unstabilized Enolates. Angewandte Chemie (International Ed. in English). e202307455 |
| Zhang P, Wang J, Robertson ZR, et al. (2022) Coordination-Controlled Nickel-Catalyzed Benzylic Allylation of Unactivated Electron-Deficient Heterocycles. Angewandte Chemie (International Ed. in English) |
| Zhang P, Huang D, Newhouse TR. (2019) Aryl-Nickel-Catalyzed Benzylic Dehydrogenation of Electron-Deficient Heteroarenes. Journal of the American Chemical Society |
| Zhang P, Li YH, Yan Z, et al. (2019) Asymmetric Total Synthesis of (-)-Pavidolide B via a Thiyl-Radical-Mediated [3+2] Annulation Reaction. The Journal of Organic Chemistry |
| Huang D, Olivieri D, Sun Y, et al. (2019) Nickel-Catalyzed Difunctionalization of Unactivated Alkenes Initiated by Unstabilized Enolates. Journal of the American Chemical Society |
| Huang D, Szewczyk SM, Zhang P, et al. (2019) Allyl-Nickel Catalysis Enables Carbonyl Dehydrogenation and Oxidative Cycloalkenylation of Ketones. Journal of the American Chemical Society |
| Zhang PP, Yan ZM, Li Y, et al. (2017) Enantioselective Total Synthesis of (-)-Pavidolide B. Journal of the American Chemical Society |
| Li S, Zhang P, Li Y, et al. (2017) Diastereoselective Synthesis of Diquinanes and Triquinanes Bearing Vicinal Quaternary Carbon Stereocenters from Acyclic Allene-based Precursors via a Cascade Reaction. Organic Letters |
| Li FZ, Li S, Zhang PP, et al. (2016) A chiral pool approach for asymmetric syntheses of (-)-antrocin, (+)-asperolide C, and (-)-trans-ozic acid. Chemical Communications (Cambridge, England) |