主要成就
{"awards": "
2007-2010 北京大学曾宪梓奖学金 2013-2014 John LaMattina Graduate Fellowship, Boston College 2014-2015 Bristol-Myers Squibb Graduate Fellowship in Synthetic Organic Chemistry 2014年国家优秀自费留学生奖学金
", "lunzhu": "
1. Meng, F.; Li, X.; Torker, S.; Shi, Y.; Hoveyda, A. H. “Catalytic Enantioselective 1,6-Conjugate Additions of Propargyl and Allyl Group,” Nature 2016, 537, 387. 2. Li, X.; Meng, F.; Torker, S.; Shi, Y.; Hoveyda, A. H. “Multicomponent Catalytic Enantioselective Conjugate Addition Reactions Involving Allylcopper Intermediates Derived from Butadiene and Isoprene,” Angew. Chem. Int. Ed. 2016, 55, 9997. 3. Meng, F.; McGrath, K. P.; Hoveyda, A. H. “Multifunctional Organoboron Compounds for Scalable Natural Product Synthesis,” Nature 2014, 513, 367. (Highlighted in Nature, Nature Chemistry and C&EN News). 4. Meng, F.; Haeffner, F.; Hoveyda, A. H. “Diastereo- and Enantioselective Reactions of Bis(pinacolato)diboron, 1,3-Enynes, and Aldehydes Catalyzed by an Easily Accessible Bisphosphine–Cu Complex,” J. Am. Chem. Soc. 2014, 136, 11304. 5. Meng, F.; Jang, H.; Jung, B.; Hoveyda, A. H. “Cu-Catalyzed Chemoselective Preparation of 2-(Pinacolato)boron-Substituted Allylcopper Complexes and their In Situ Site-, Diastereo-, and Enantioselective Additions to Aldehydes and Ketones,” Angew. Chem., Int. Ed. 2013, 52, 5046. 6. Meng, F.; Jung, B.; Haeffner, F.; Hoveyda, A. H. “NHC–Cu-Catalyzed Protoboration of Monosubstituted Allenes. Ligand-Controlled Site Selectivity, Application to Synthesis and Mechanism,” Org. Lett. 2013, 15, 1414. 7. Meng, F.; Jang, H.; Hoveyda, A. H. “Exceptionally E- and β-Selective NHC–Cu-Catalyzed Proto-Silyl Addition to Terminal Alkynes and Site- and Enantioselective Proto-Boryl Additions to the Resulting Vinylsilanes: Synthesis of Enantiomerically Enriched Vicinal and Geminal Borosilanes,” Chem. Eur. J. 2013, 19, 3204. 8. Ren, W.; Chen, Z.; Xiao, Q.; Li, Y.; Sun, T.; Zhang, Z.; Ye, Q.; Meng, F.; You, L.; Zhao, M.; Xu, L.; Tang, Y.; Chen, J.; Yang, Z. “Diastereoselective Total Synthesis of (±)-Schindilactone A, Part 3: The Final Phase and Completion,” Chem. Asian J. 2012, 7, 2341. 9. Li, Y.; Chen, Z.; Xiao, Q.; Ye, Q.; Sun, T.; Meng, F.; Ren, W.; You, L.; Xu, L.; Wang, Y.; Chen, J.; Yang, Z. “Diastereoselective Total Synthesis of (±)-Schindilactone A, Part 2: Construction of the Fully Functionalized CDEFGH Ring System,” Chem. Asian J. 2012, 7, 2334. 10. Sun, T.; Ren, W.; Xiao, Q.; Tang, Y.; Zhang, Y.; Li, Y.; Meng, F.; Liu, Y.; Zhao, M.; Xu, L.; Chen, J.; Yang, Z. “Diastereoselective Total Synthesis of (±)-Schindilactone A, Part 1: Construction of the ABC and FGH Ring Systems and Initial Attempts to Construct the CDEF Ring System,” Chem. Asian J. 2012, 7, 2321. 11. Xiao, Q.; Ren, W.; Chen, Z.; Sun, T.; Li, Y.; Ye, Q.; Gong, J.; Meng, F.; You, L.; Liu, Y.; Zhao, M.; Xu, L.; Shan, Z.; Shi, Y.; Tang, Y.; Chen, J.; Yang, Z. “Diastereoselective Total Synthesis of (±)-Schindilactone A,” Angew. Chem., Int. Ed. 2011, 50, 7373. 12. Xiao, Q.; Wang, W.; Liu, G.; Meng, F.; Chen, J.; Yang, Z.; Shi, Z. “Direct Imidation to Construct 1H-Benzo[d]imidazole through Pd(II)-Catalyzed C–H Activation Promoted by Thiourea,” Chem. Eur. J. 2009, 15, 7292.
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