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Publications （发表论文）
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2015:
23. Radical CationSalt-Promoted Catalytic Aerobic sp3 C−H Oxidation: Construction of Quinoline-Fused Lactones and Lactams J. Org. Chem. 2015, 80, 609 (IF:4.564, SC-II)
http://pubs.acs.org/doi/pdf/10.1021/jo502184k
22. Oxidative Povarov Reaction via sp3 C−H Oxidation of N-Benzylanilines Induced by Catalytic Radical Cation Salt: Synthesis of 2,4-Diarylquinoline Derivatives Org. Lett.2015, 17, 1409 (IF: 6.324,SCI-II)
http://pubs.acs.org/doi/pdf/10.1021/acs.orglett.5b00244
2014：
21. Catalytic aromatizationof 1,4-dihydropyridines by radical cation salt prompted aerobic oxidation TetrahedronLett.2014, 55, 264 (IF: 2.391, SCI-III)
20. Cerium(IV)-Catalyzed sp3 C-H Bond Oxidation of Glycine Derivatives: Radical Cation Prompted Dioxygen Activation in the Presence of Triarylamine Adv.Synth. & Catal.2014, 356, 3214（IF：5.542；SCI-II）
19. Catalytic Oxidation of C(sp3)-H Bonds Induced by a Radical Cation Salt: Construction of 1,4-Dihydropyridines Using a Fragment-Reassembly Strategy Adv. Synth. & Catal.2014, 356,1210（IF: 5.542, SCI-II）
18. Brominationof Arenes Using I2O5-KBr in Water Synth. Comm.2014, 44, 181（SCI-III）
2013:
17. Catalytic sp3 C−H Oxidation of Peptides and Their Analogues by Radical Cation Salts: From Glycine Amides to Quinolines J. Org. Chem. 2013, 78, 9450（IF:4.564, SCI-II）
16. Synthesis of 2,3-disubstituted quinolines fromin situ generated imines and its enamine tautomer under radical cation induced conditions Tetrahedron Lett. 2013,54, 4950.（IF: 2.397, SCI-III）
2012:
15. A Conjunctive Carboiodination: Indenes by aDouble Carbopalladation–Reductive Elimination Domino Process Angew. Chem. Int. Ed. 2012, 51, 9870（IF：11.829, SCI-I）
14. CatalyticRadical Cation Salt Induced Csp3-H Functionalization of Glycine Derivatives: Synthesis of Substituted Quinolines Org. Lett. 2012, 14, 4030（IF:5.862, SCI-II）
13. Radical cation salt induced Povarov reactionbetween iminoethyl glyoxylate and N-vinylamides: synthesis ofquinoline-2-carboxylate derivatives Tetrahedron Lett.2012,53, 7140（IF:2.683, SCI-III）
12. Cross double Mannich reaction induced by I2: synthesis of highly subtituted 4-piperidones Chinese Chemical Letters 2012，23，309（IF: 0.643, SCI-III）
11. Synthsis of4-Piperidones via Multicomponent Double Mannich Reaction Catalyzed by I2 ChineseJournal of Chemistry 2012, 30, 1504（IF：0.891, SCI-III）
2011:
10. Double Mannich Reaction and Tandem Cyclization of Imines with Ketones Catalyzed by InCl3·4H2O: Stereoselective Synthesis of Highly Substituted 4-Piperidones Adv. Synth. Catal.2011, 353,315（IF: 5.187, SCI-II）
9. I2-InducedStereospecific Synthesis of 4-Piperidones through Double Mannich Reaction and Tandem Cyclization Eur. J. Org. Chem. 2011, 1627（IF:3.096, SCI-III）
8. Radical Cation Salts Induces Domino Reaction of Anilines with Enol Ethers：Synthesis of 1,2,3,4-Tetrahrdroquinoline Derivatives Chin.Chem. Lett. 2011, 22, 671（IF: 0.643, SCI-III）
2010:
7. Synthesis of b-Aminoketones and Construction of Highly Substituted 4-Piperidones by Mannich Reaction Induced by Persistent RadicalCation Salts Org. Lett.2010, 12, 732（IF: 5.420, SCI-I）
6. Mannich Reaction of Imines and Silyl Enol Ethers Induced by Radical Cation Salts: Synthesis of b-Aminoketones Synlett 2010, 2964（IF: 2.718, SC-III）
5. Radical cationsalt induced tandem cyclization between anilines and N-vinyl amides: synthesis of 2-methyl-4-anilino-1,2,3,4-tetrahydroquinoline derivatives TetrahedronLett. 2010, 51, 6779（IF: 2.660；SCI-III）
2009:
4. Synthesisof Oxime Ether under Single Electron Oxidation Induced by Radical Cation Tris(aryl)aminium Salts. O-Alkylation of Oxime with N-Vinyllactam，Tetrahedron 2009, 65, 2334-2338. (IF: 2.897, SCI-III)
2008:
3. O-Alkylation of Oxime with N-Vinyl Lactams Induced by Radical Cation，Tetrahedron Lett. 2008, 49, 1786. (IF: 2.538,SCI-III)
2006:
2. Cation Radical Aza-Diels-Alder Reaction between N-Arylimines and N-Vinyllactams: A Facile Synthesis of 4-Lactam-N-yl Tetrahydroquinolines，Synthesis 2006, 2831. (IF: 2.203, SCI-III)
2003:
1.Cation Radical Imino Diels-Alder Reaction：A New Approach for the Synthesis of Tetrahydroquinolines，Synlett 2003, 1707. (IF:2.741, SCI-III)
https://blog.sciencenet.cn/blog-459724-941898.html
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