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成果及论文

[1] Tan, L.; Chen, J.; Liu, X.; Matler, A.; Schopper, N.; Finze, M.; Lin, Z.; Ye, Q.; Antiaromatic 2-Azaboroles with π4σ2 Electronic Configuration, J. Am. Chem. Soc. 2024, 10.1021/jacs.4c10145, (共同第一作者).

[2] Wang, J.; Xiang, L.; Liu, X.; Matler, A.; Lin, Z.; Ye, Q.; Avenue to novel o-carboranyl boron compounds – reactivity study of o-carborane-fused aminoborirane towards organic azides, Chem. Sci. 2024, 15, 4839-4845.

[3] Liu, X.; Heinz, M.; Wang, J.; Tan, L.; Holthausen, M. C.; Ye, Q.; A Journey from Benzoborirene to Benzoborole-Supported 1,2-Diimine and Antiaromatic Borolediide, Angew. Chem. Int. Ed. 2023, 62, e202312608.

[4] Zhang, C.; Liu, X.; Wang, J.; Ye, Q.; A Three-Dimensional Inorganic Analogue of 9,10-Diazido-9,10-Diboraanthracene: A Lewis Superacidic Azido Borane with Reactivity and Stability, Angew. Chem. Int. Ed. 2022, 61, e202205506.

[5] Ming, W.; Soor, H. S.; Liu, X.; Trofimova, A.; Yudin, A. K.; Marder, T. B.; α-Aminoboronates: recent advances in their preparation and synthetic applications, Chem. Soc. Rev. 2021, 50, 12151-12188.

[6] Ming, W.; Liu, X.; Mao, L.; Gu, X.; Ye, Q.; Transition-Metal-Catalyzed Synthesis of Chiral Allylboronates, Chin. J. Chem . 2021, 39, 1716-1725.

[7] Ming, W.; Liu, X.; Friedrich, A.; Krebs, J.; Marder, T. B.; The Borono–Strecker Reaction: Synthesis of α-Aminoboronates via a Multicomponent Reaction of Carbonyl Compounds, Amines, and B2pin2, Org. Lett. 2020, 22, 365-370.

[8] Ming, W.; Liu, X.; Friedrich, A.; Krebs, J.; Budiman, Y. P.; Huang, M.; Marder, T. B.; Concise Synthesis of α-Amino Cyclic Boronates via Multicomponent Coupling of Salicylaldehydes, Amines, and B2(OH)4, Green Chem. 2020, 22, 2184-2190.

[9] Liu, X.; Ming, W.; Luo, X.; Friedrich, A.; Maier, J.; Radius, U.; Santos, W. L.; Marder, T. B.; Regio- and Stereoselective Synthesis of 1,1-Diborylalkenes via Brønsted Base-Catalyzed Mixed Diboration of Alkynyl Esters and Amides with BpinBdan, Eur. J. Org. Chem. 2020, 2020, 1941-1946.

[10] Liu, X.; Ming, W.; Friedrich, A.; Kerner, F.; Marder, T. B.; Copper-Catalyzed Triboration of Terminal Alkynes Using B2pin2: Efficient Synthesis of 1,1,2-Triborylalkenes, Angew. Chem. Int. Ed. 2020, 59, 304-309.

[11] Liu, X.; Ming, W.; Zhang, Y.; Friedrich, A.; Marder, T. B.; Copper-Catalyzed Triboration: Straightforward, Atom-Economical Synthesis of 1,1,1-Triborylalkanes from Terminal Alkynes and HBpin, Angew. Chem. Int. Ed. 2019, 58, 18923-18927.

[12] Wang, L.; Liu, X.; Wang, M.; Liu, J.; Copper(I)-Catalyzed Heterocyclization of α-Acyl-α-alkynyl Ketene Dithioacetals: Synthesis of 3-Cyanofurans, Org. Lett. 2016, 18, 2162-2165.

[13] Ming, W.; Liu, X.; Wang, L.; Liu, J.; Wang, M.; Tandem Thien- and Benzannulations of α-Alkenoyl-α-alkynyl Ketene Dithioacetals with Cyanoacetates: Synthesis of Functionalized Benzo[b]thiophenes, Org. Lett. 2015, 17, 1746-1749.

[14] Liu, B.; Zheng, G.; Liu, X.; Xu, C.; Liu, J.; Wang, M.; Regio- and Stereoselective Synthesis of 2-Cyclopentenones via a Hydrogenolysis-Terminated Heck Cyclization of β-Alkylthio Dienones, Chem. Commun. 2013, 49, 2201-2203.