Dianhu Zhu
Affiliations: | 2006-2010 | Shandong Agricultural University | |
| 2010-2013 | Shenyang Research Institute of Chemical Industry | ||
| 2013-2016 | SIOC,CAS | ||
| 2016-2017 | California Institute of Technology, Pasadena, CA | ||
| 2017-2019 | McGill University, Montreal, QC, Canada | ||
| 2019- | Northwest University, Xi'an, China |
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Parents
Sign in to add mentor| Qilong Shen | grad student | 2013-2016 | SIOC,CAS |
| Brian M. Stoltz | post-doc | 2016-2017 | Caltech |
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Publications
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| Wang S, Yang L, Liang F, et al. (2023) Synthetic exploration of electrophilic xanthylation powerful -xanthylphthalimides. Chemical Science. 14: 9197-9206 |
| Zhu D, Lv L, Qiu Z, et al. (2019) Nickel-Catalyzed Cross-Coupling of Umpolung Carbonyls and Alkyl Halides. The Journal of Organic Chemistry |
| Lv L, Zhu D, Li CJ. (2019) Direct dehydrogenative alkyl Heck-couplings of vinylarenes with umpolung aldehydes catalyzed by nickel. Nature Communications. 10: 715 |
| Li C, Huang J, Dai X, et al. (2019) An Old Dog with New Tricks: Enjoin Wolff–Kishner Reduction for Alcohol Deoxygenation and C–C Bond Formations Synlett. 30: 1508-1524 |
| Lv L, Zhu D, Qiu Z, et al. (2019) Nickel-Catalyzed Regioselective Hydrobenzylation of1,3-Dienes with Hydrazones Acs Catalysis. 9: 9199-9205 |
| Zhu D, Lv L, Li CC, et al. (2018) Umpolung Carbonyl Groups as Alkyl Organometallic Reagent Surrogates for Palladium Catalyzed Allylic Alkylation. Angewandte Chemie (International Ed. in English) |
| Li J, Zhu D, Lv L, et al. (2018) Radical difluoromethylthiolation of aromatics enabled by visible light. Chemical Science. 9: 5781-5786 |
| Li CC, Dai XJ, Wang H, et al. (2018) Iron-Catalyzed Nucleophilic Addition Reaction of Organic Carbanion Equivalents via Hydrazones. Organic Letters |
| Lv L, Zhu D, Tang J, et al. (2018) Cross-Coupling of Phenol Derivatives with Umpolung Aldehydes Catalyzed by Nickel Acs Catalysis. 8: 4622-4627 |
| Zhu D, Hong X, Li D, et al. (2017) A Two-Step, One-Pot, and Multigram-Scale Synthesis of N-Difluoromethylthiophthalimide Organic Process Research & Development. 21: 1383-1387 |