近期论文
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1.“Organohalogenite-Catalyzed Spiroketalization: Enantioselective Synthesis of Bisbenzannulated Spiroketal Cores.” Xue, J.*; Zhang, H.; Tian, T.; Yin, K.; Liu, D.; Jiang, X.*; Li, Y.*; Jin, X.; Yao, X. Adv. Synth. Catal. 2016, 358, 370-374.
2.“Alkynylation/Dearomatizative Cyclization to Construct Spiro 5.5 Undecanes.”Shao, J.; Li, L.*; Zhang, J.; Hu, J.; Xue, J.; Li, Y.* RSC Adv. 2016, 6, 31363-31366.
3.“Mg(ClO4)2-Promoted [4 + 3] Cycloaddition of Oxindole Derivatives with Conjugated Dienes: Concise Synthesis of Spirocycloheptane Oxindole Derivatives.”Liu, Y.; Sun, Z.; Li, S.; Xiang, K.; Zhang, Y.*; Li, Y.* RSC Adv. 2016, 6, 26954-26958.
4.“TMSI-Promoted Vinylogous Michael Addition of Siloxyfuran to 2-Substituted Chromones: A General Approach for the Total Synthesis of Chromanone Lactone Natural Products.”Liu, J.; Li, Z.; Tong, P.; Xie, Z.; Zhang, Y.*; Li, Y.* J. Org. Chem. 2015, 80, 1632-1643.
5.“Enantioselective Syntheses of Spiroketals via a Tandem Reaction of Cu(I)-Catalyzed Cycloetherification and Hydrogen-Bond-Induced [4+2] Cyclization.”Tian, T.; Li, L.; Xue, J.; Zhang, J.; Li, Y. J. Org. Chem. 2015, 80, 4189–4200.
6.“One Pot Hydroamination/ 4+3 Cycloaddition: Synthesis towards the Cyclohepta b Indole Core of Silicine and Ervatamine.”Zhang, J.; Shao, J.; Xue, J.*; Wang, Y.; Li, Y.* RSC Adv. 2014, 4, 63850-63854.
7.“Total Synthesis of Aphadilactones A–D.”Yin, J.-P.; Gu, M.; Li, Y.*; Nan, F.-J.* J. Org. Chem. 2014, 79, 6294-6301.
8.“Ivorenolide B, An Immunosuppressive 17-Membered Macrolide from Khaya ivorensis: Structural Determination and Total Synthesis.”Wang, Y.; Liu, Q.-F.; Xue, J.-J.; Zhou, Y.; Yu, H.-C.; Yang, S.-P.; Zhang, B.; Zuo, J.-P.; Li, Y.*; Yue, J.-M.* Org. Lett. 2014, 16, 2062-2065.
9.“Total Synthesis of (+/-)-delta-Rubromycin.”Wang, W.; Xue, J.*; Tian, T.; Zhang, J.; Wei, L.; Shao, J.; Xie, Z.; Li, Y.* Org. Lett. 2013, 15, 2402-2405.
10.“The First Asymmetric Total Synthesis of (+)-Coriandrone A and B.”Wang, W.; Xue, J.*; Tian, T.; Jiao, Y.; Li, Y.* Org. Biomol. Chem. 2013,11, 6686-6690.
11.“Regio- and Stereoselective 4+3 Cycloaddition Towards Fused 5,7,6-Tricyclic Skeletons.”Gong, W.; Liu, Y.; Zhang, J.; Jiao, Y.; Xue, J.*; Li, Y.* Chem. Asian J. 2013, 8, 546-551.
12.“A Novel, Facile Approach to Frondosin B and 5-epi-Liphagal via a New 4+3 -Cycloaddition.”Zhang, J.; Li, L.; Wang, Y.; Wang, W.; Xue, J.*; Li, Y.* Org. Lett. 2012, 14, 4528-4530.
13.“Ivorenolide A, an Unprecedented Immunosuppressive Macrolide from Khaya ivorensis: Structural Elucidation and Bioinspired Total Synthesis.”Zhang, B.; Wang, Y.; Yang, S.-P.; Zhou, Y.; Wu, W.-B.; Tang, W.; Zuo, J.-P.; Li, Y.*; Yue, J.-M.* J. Am. Chem. Soc. 2012, 134, 20605-20608.
14.“Construction of Aromatic 5, 5 Spiroketals via Hypoiodite-Catalyzed Etherification Combined in Relay Cascades.”Wei, W.; Wang, Y.; Yin, J.; Xue, J.*; Li, Y.* Org. Lett. 2012, 14, 1158-1161.
15.“New Fluoride-Promoted Hypoiodite-Catalytic Oxidative Cycloetherification to Aromatic Spiroketals.”Wei, W.; Li, L.; Lin, X.; Li, H.; Xue, J.*; Li, Y.* Org. Biomol. Chem. 2012, 10, 3494-3499.
16.“Synthesis of (+/-)-gamma-Rubromycin via a New Hypoiodite-Catalytic Oxidative Cycloetherification.”Wei, L.; Xue, J.*; Liu, H.; Wang, W.; Li, Y.* Org. Lett. 2012, 14, 5302-5305.
17.“Copper(I)-Catalyzed Hydroalkoxylation/Hydrogen-Bonding-Induced Asymmetric Hetero-Diels-Alder Cycloaddition Cascade: An Approach to Aromatic Spiroketals.” Li, X.; Xue, J.*; Huang, C.; Li, Y. Chem. Asian J. 2012, 7, 903-906.
18.“Construction of Two Vicinal Quaternary Carbons by Asymmetric Allylic Alkylation: Total Synthesis of Hyperolactone C and (-)-Biyouyanagin A.”Du, C.; Li, L.; Li, Y.; Xie, Z.* Angew. Chem., Int. Edit. 2009, 48 , 7853-7856.
19. ”An Efficient Synthesis of Highly Functionalized 5,6 Aromatic Spiroketals by Hetero-Diels-Alder Reaction.”Zhou, G.; Zhu, J.; Xie, Z.*; Li, Y.* Org. Lett. 2008, 10, 721-724.
20. “Total Synthesis of (+/-)-Quadrangularin A.”Li, W.; Li, H.; Li, Y.; Hou, Z.* Angew. Chem., Int. Edit. 2006, 45, 7609-7611.