代表性论文: Postdoc Works @ UCR (University of California, Riverside) 1. Hai-Bin Yang, Abigail Feceu, David B. C. Martin*, Catalyst-Controlled C-H Functionalization of Adamantanes using Selective H-Atom Transfer. ACS Catal. 2019, 9, 5708-5715. (IF = 11.384). Postdoc Works @ SU (Stockholm University) 2. Hai-Bin Yang, Stalin R. Pathipati, Nicklas Selander*, Nickel-Catalyzed 1,2-Aminoarylation of Oxime Ester-Tethered Alkenes with Boronic Acids. ACS Catal. 2017, 7, 8441-8445. (IF = 11.384). 3. Hai-Bin Yang, Nicklas Selander*, Divergent Iron-Catalyzed Coupling of O-Acyloximes with Silyl Enol Ethers. Chem. Eur. J. 2017, 23, 1779-1783. (IF = 5.16) Highlighted in Synfacts (2017, 13, 0350); Highly cited paper. 4. Hai-Bin Yang, Nicklas, Selander*, A redox-economical synthesis of trifluoromethylated enamides with the Langlois reagent. Org. Biomol. Chem. 2017, 15, 1771-1775. (IF = 3.423) Doctoral works @ SIOC (Shanghai Institute of Organic Chemistry) 5. Hai-Bin Yang, Yu-Chao Yuan, Yin Wei*, Min Shi*, Amine-catalyzed tunable reactions of allenoates with dithioesters: formal [4+2] and [2+2] cycloadditions for the synthesis of 2,3-dihydro-1,4-oxathiines and enantioenriched thietanes. Chem. Commun. 2015, 51, 6430-6433. (IF = 6.290) 6. Hai-Bin Yang, Yun-Zhou Zhao, Rui Sang, Yin Wei*, Min Shi*, Asymmetric Synthesis of Bioxindole‐Substituted Hexahydrofuro[2,3-b]furans via Hydroquinine Anthraquinone-1,4-diyl Diether-Catalyzed Domino Annulation of Acylidenoxindoles/Isatins, Acylidenoxindoles and Allenoates. Adv. Synth. Catal. 2014, 356, 3799-3808. (IF = 5.123) 7. Hai-Bin Yang, Yun-Zhou Zhao, Rui Sang, Min Shi*, (DHQ)2AQN-Catalyzed Asymmetric Substitution of Isatin-Derived Hydrazones with O-Boc-Protected Morita-Baylis-Hillman Adducts: A Strategy for Synthesizing Enantioenriched Azo Compounds Incorporating an Oxindole Scaffold. J. Org. Chem. 2014, 79, 3519-3528. (IF = 4.805) 8. Hai-Bin Yang, Xing Fan, Yin Wei*, Min Shi*, Solvent-controlled nucleophilic trifluoromethylthiolation of Morita–Baylis–Hillman carbonates: dual roles of DABCO in activating the Zard's trifluoromethylthiolation reagent and the MBH carbonates. Org. Chem. Front. 2015, 2, 1088-1093. (IF = 5.455) 9. Hai-Bin Yang, Xiao-Yang Guan, Yin Wei, Min Shi*, A Three-Component Condensation for the Construction of the Spiro[indoline-3,3’-piperidin]-2-one Skeleton. Eur. J. Org. Chem. 2012, 2792-2800. (IF = 2.882) 10. Hai-Bin Yang, Yun-Zhou Zhao, Rui Sang, Xiang-Yin Tang, Min Shi*, A novel multicomponent reaction involving isoquinoline, allenoate and activated ketone. Tetrahedron, 2013, 69, 9205-9211. (IF = 2.377) 11. Hai-Bin Yang, Yin Wei*, Min Shi*, Construction of spiro[indoline]oxindoles through one-pot thermal-induced [3+2] cycloaddition/silica gel-promoted fragmentation sequence between isatin ketonitrones and electron-deficient alkynes. Tetrahedron, 2013, 69, 4088-4097. (IF = 2.377) 12. Hai-Bin Yang, Min Shi*, Yb(NTf2)3-catalyzed [3+3] cycloaddition between isatin ketonitrones and cyclopropanes to construct novel spiro[tetrahydro-1,2-oxazine]oxindoles. Org. Biomol. Chem. 2012, 10, 8236-8243. (IF = 3.423) 13. Long Huang, Hai-Bin Yang, Di-Han Zhang, Zhen Zhang, Xiang-Ying Tang, Qin Xu,* Min Shi*, Gold-Catalyzed Intramolecular Regio- and Enantioselective Cycloisomerization of 1,1-Bis(indolyl)-5-alkynes. Angew. Chem. Int. Ed. 2013, 52, 6767-6771. (IF = 12.102) 14. Yun-Zhou Zhao, Hai-Bin Yang, Xiang-Ying Tang*, Min Shi*, RhII-Catalyzed [3+2] Cycloaddition of 2 H-Azirines with N-Sulfony-1,2,3-Triazoles. Chem. Eur. J. 2015, 21, 3562-3566. (IF = 5.16) 15. Yu-Chao Yuan, Hai-Bin Yang, Xiang-Ying Tang,* Yin Wei,* and Min Shi*, Unprecedented Oxycyanation of Methylenecyclopropanes for the Facile Synthesis of Benzoxazine Compounds Containing a Cyano Group. Chem. Eur. J. 2016, 22, 5146-5150. (IF = 5.16) 16. Xing Fan, Haibin Yang, Min Shi*, Tertiary Amine-Catalyzed Difluoromethylthiolation of Morita-Baylis-Hillman Carbonates of Isatins with Zard's Trifluoromethylthiolation Reagent. Adv. Synth. Catal. 2017, 359, 49-57. (IF = 5.123) 17. Rui Sang, Hai-Bin Yang, Min Shi*, DBU-mediated transformation of arylmethylenecyclopropenes to alkylidenecyclopropanes. Tetrahedron Lett. 2013, 54, 3591-3594. (IF = 2.125) |