论文著作:
1. “Recent Development and Applications of Semipinacol Rearrangement Reactions.” Zhang, X.-M.; Li, B.-S.;* Wang, S.-H.;* Zhang, K.; Zhang, F.-M.; Tu, Y.-Q. Chem. Sci. 2021, 12, 9262–9274.
2. “Catalytic Enantioselective Synthesis of Chiral Spirocyclic 1,3-Diketones via Organo-Cation Catalysis.” Zhang, X.-Y.; Shao, Y.-P.; Guo, B.-K.; Zhang, K.; Zhang, F.-M.; Zhang, X.-M.;* Tu, Y.-Q.* Chem. Commun. 2021, 57, 11233–11235.
3. “Collective Total Synthesis of Aspidofractinine Alkaloids through the Development of a Bischler–Napieralski/Semipinacol Rearrangement Reaction.” Wang, S.-H.; Si, R.-Q.; Zhuang, Q.-B.; Guo, X.; Ke, T.; Zhang, X.-M.;* Zhang, F.-M.;* Tu, Y.-Q.* Angew. Chem., Int. Ed. 2020, 59, 21954–21958.
4. “Enantioselective Catalytic Aldehyde α-Alkylation/Semipinacol Rearrangement: Construction of α-Quaternary-δ-Carbonyl Cycloketones and Total Synthesis of (+)-Cerapicol.” Yang, J.; Zhang, X.-M.;* Zhang, F.-M.; Wang, S.-H.; Tu, Y.-Q.;* Li, Z.; Wang, X.-C.; Wang H. Angew. Chem., Int. Ed. 2020, 59, 8471–8475.
5. “Allylic Arylation of 1,3-Dienes via Hydroboration/Migrative Suzuki−Miyaura Cross-Coupling Reactions.” Zhang, X.-M.;* Yang, J.; Zhuang, Q.-B.; Tu, Y.-Q.; Chen, Z.; Shao, H.; Wang, S.-H.; Zhang, F.-M. ACS Catal. 2018, 8, 6094-6099.
6. “A Catalytic Allylic Cation-Induced Intermolecular Allylation-Semipinacol Rearrangement.” Xu, M.-H.; Dai, K.-L.; Tu, Y.-Q.;* Zhang, X.-M.;* Zhang, F.-M.; Wang, S.-H. Chem. Commun. 2018, 54, 7685-7688.
7. “Recent Applications of the 1,2-Carbon Atom Migration Strategy in Complex Natural Product Total Synthesis.” Zhang, X.-M.; Tu, Y.-Q.;* Zhang, F.-M.; Chen, Z.-H.; Wang, S.-H.* Chem. Soc. Rev. 2017, 46, 2272-2305.
8. “Radical Aryl Migration Reactions and Synthetic Applications.” Chen Z.-M.;# Zhang X.-M.;# Tu Y.-Q.* Chem. Soc. Rev. 2015, 44, 5220-5245. (equal contribution)
9. “Total Synthesis of (+)-Alopecuridine, (+)-Sieboldine A, and (-)-Lycojapodine A.” Zhang X.-M.; Shao H.; Tu Y.-Q.;* Zhang F.-M.; Wang S.-H.* J. Org. Chem. 2012, 77, 8174-8181.
10. “Total Synthesis of (±)-Alopecuridine and Its Biomimetic Transformation into (±)-Sieboldine A.” Zhang X.-M.; Tu Y.-Q.;* Zhang F.-M.; Shao H.; Meng X. Angew. Chem., Int. Ed. 2011, 50, 3916-3919.