Fang Liu
Affiliations: | Nanjing Agricultural University |
Area:
computational chemistryGoogle:
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Publications
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| Han C, Zhao F, Lu Q, et al. (2023) Computational Determination of the Mechanism of the Palladium-Catalyzed Domino Reaction of -Iodostyrene, Oxanorbornadiene, and Phenylboronic Acid. The Journal of Organic Chemistry. 88: 15608-15614 |
| Niwa K, Ohashi M, Xie K, et al. (2023) Biosynthesis of Polycyclic Natural Products from Conjugated Polyenes via Tandem Isomerization and Pericyclic Reactions. Journal of the American Chemical Society. 145: 13520-13525 |
| Sengupta A, Li B, Svatunek D, et al. (2022) Cycloaddition Reactivities Analyzed by Energy Decomposition Analyses and the Frontier Molecular Orbital Model. Accounts of Chemical Research |
| Yahiaoui O, Murray LAM, Zhao F, et al. (2022) A Diazo-Hooker Reaction, Inspired by the Biosynthesis of Azamerone. Organic Letters |
| Zhao F, Yu P, Chen Y, et al. (2021) π-Facial Stereoselectivity in Acyl Nitroso Cycloadditions to 5,5-Unsymmetrically Substituted Cyclopentadienes: Computational Exploration of Origins of Selectivity and the Role of Substituent Conformations on Selectivity. The Journal of Organic Chemistry |
| Ramirez M, Svatunek D, Liu F, et al. (2021) Origins of Endo Selectivity in Diels-Alder Reactions of Cyclic Allene Dienophiles. Angewandte Chemie (International Ed. in English) |
| Chen PP, Ma P, He X, et al. (2021) Computational Exploration of Ambiphilic Reactivity of Azides and Sustmann's Paradigmatic Parabola. The Journal of Organic Chemistry |
| Lowder L, Zhao F, Vaughan MM, et al. (2020) Diversification of Nucleophile-Intercepted Beckmann Fragmentation (NuBFr) Products and Related DFT Studies. The Journal of Organic Chemistry |
| Houk KN, Liu F, Yang Z, et al. (2020) Evolution of the Diels-Alder Reaction Mechanism Since the 1930s: Woodward, Houk with Woodward, and the Influence of Computational Chemistry on Understanding Cycloadditions. Angewandte Chemie (International Ed. in English) |
| Houk KN, Liu F, Chen Y. (2020) Huisgen's 1,3-Dipolar Cycloadditions to Fulvenes via Ambimodal [6+4]/[4+2] Transition States. Angewandte Chemie (International Ed. in English) |