近期论文
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1) “Synthetic Study Toward the Misassigned (±)-Tronoharine”, Z. Xue, Y. Li, J. Zhang, F.-S. Han,* Org. Lett., in press.
2) “Palladium-Catalyzed Enantioselective Synthesis of P-Stereogenic Phosphinamides via Desymmetric C–H Arylation”, Z.-J. Du, J. Guan, G.-J. Wu, P. Xu, L.-X. Gao, F.-S. Han,* J. Am. Chem. Soc., in press.
3) “Formal [3+3] Cyclization of Indol-2-yl Carbinol with Aza-Diene and the Subsequent Oxidative Ring Expansion Reaction for the Synthesis of Indole Azepinones”, X. Zhong, Y. Li, W.-X. Zhang, J. Zhang, S.-X. Wang, F.-S. Han,* Chem. Commun., 2014, 50, 11181.
4) “Chiral Phosphoramide-Catalyzed Enantioselective Synthesis of 2,3’-Diindoylarylmethanes from Indol-2-yl Carbinol and Indole”, S. Qi, C.-Y. Liu, J.-Y. Ding, F.-S. Han,* Chem. Commun., 2014, 50, 8605.
5) “Palladium-Catalyzed Silver-Mediated α-Arylation of Acetic acid: A New Approach for the α-Arylation of Carbonyl Compounds”, G.-J. Wu, J. Guan, F.-S. Han,* Y.-L. Zhao,* ChemCatChem, 2014, 6, 1589.
6) “Cu-Mediated Direct Aryl C–H Halogenation: a Strategy to Control Mono- and Di-Selectivity”, Z.-J. Du, L.-X. Gao, Y.-J. Lin, F.-S. Han,* ChemCatChem, 2014, 6, 123–126.
7) “Pd(II)-Catalyzed Mild C–H ortho Arylation and Intramolecular Amination Oriented by Phosphinamide Group”, J. Guan, G.-J.Wu, F.-S. Han,* Chem. Eur. J., 2014, 20, 3301.
8) “The Development of Copper-Catalyzed Aerobic Oxidative Coupling of H-Tetrazoles with Boronic Acids and an Insight into the Reaction Mechanism”, C.-Y. Liu, Y. Li, J.-Y. Ding, D.-W. Dong, F.-S. Han,* Chem. Eur. J., 2014, 20, 2373–2381.
9) “Copper-Mediated Direct Aryl C–H Cyanation with Azobisisobutyro-nitrile via a Free-radical Pathway”, H. Xu, P.-T. Liu, Y.-H. Li, F.-S. Han,* Org. Lett., 2013, 15, 3354.
10) “Transition-Metal-Catalyzed Suzuki-Miyaura Cross-Coupling Reactions: A Remarkable Advance from Palladium to Nickel Catalysts”, F. Han,* Chem. Soc. Rev., 2013, 42, 5270. (Invited review).
11) “Iron-Catalyzed Direct Synthesis of Densely Substituted Benzofurans and Naphthopyrans from Phenolic Compounds and Propargylic Alcohols” F.-Q. Yuan, F. Han*, Adv. Synth. Catal., 2013, 355, 537.
12) “Al-Catalyzed Facile Construction of Quaternary C–C Bonds via the Allylic Substitution of tertiary Alcohols: A Concise Formal Synthesis of (±)-Mersicarpine”, X. Zhong, Y. Li, F. Han*, Chem. Eur. J., 2012, 18, 9784.
13) “Ni-Catalyzed Construction of C–P Bond from Electron-deficient Phenols via the in situ Aryl C–O Activation by PyBroP”, Y.-L. Zhao, G.-J. Wu, F. Han*, Chem. Commun., 2012, 48, 5868.
14) “Ni(dppp)-Catalyzed Cross-coupling of Aryl Halides with Dialkylphosphite, Diphenylphosphine oxide, and Diphenylphosphine”, Y.-L. Zhao, G.-J. Wu, Y. Li, L.-X. Gao, F. Han*, Chem. Eur. J., 2012, 18, 9622.
15) “Synthesis of Densely Substituted a,b,g,d-Dienones via the PdII-Catalyzed Allylation, H-Migration, and Aerobic Oxidative d-Hydride Elimination Cascade”, F.-Q. Yuan, F. Han*, Org. Lett., 2012, 14, 1218.
16) “Efficient Synthesis of 2,5-Disubstituted Tetrazoles via the Cu2O-Catalyzed Aerobic Oxidative Direct Cross-coupling of N-H Free Tetrazoles with Boronic Acids”, Y. Li, L.-X. Gao, F. Han*, Chem. Commun., 2012, 48, 2719.
17) “PdCl2(dppf)-Catalyzed in situ Coupling of 2-Hydroxypyridines with Aryl Boronic Acids Mediated by PyBroP and the one-pot Chemo- and Regioselective Construction of two Distinct Aryl-Aryl Bonds”, S.-M. Li, J. Huang, G.-J. Chen, F. Han*, Chem. Commun., 2011, 47, 12840.
18) “PdCl2-Catalyzed Efficient Allylation and Benzylation of Heteroarenes under Ligand, Base/Acid, and Additive-Free Conditions”, F.-Q. Yuan, L.-X. Gao, F. Han*, Chem. Commun., 2011, 47, 5289.
19) “Ni-Catalyzed Cross-Coupling of Phenols and Aryl Boronic Acids via an in situ Phenol Activation Mediated by PyBrOP”, G. J. Chen, J. Huang, L. X. Gao, F. Han*, Chem. Eur. J., 2011, 17, 4038.
20) “A Highly Practical and Reliable Nickel Catalyst for Suzuki-Miyaura Coupling of Aryl Halides” Y.-L. Zhao, Y. Li, S.-M. Li, Y.-G. Zhou, F.-Y. Sun, L.-X. Gao, F.-S. Han*, Adv. Synth. Catal., 2011, 353, 1543.
21) “Highly Efficient Suzuki-Miyaura Coupling of Aryl Tosylates and Mesylates Catalyzed by Stable, Cost-effective [1,3-Bis(diphenylphosphino)propane]nickel(II) Chloride {Ni(dppp)Cl2} with only 1 mol % Loading”, H. Gao, Y. Li, Y. G. Zhou, F. Han,* Y. J. Lin*, Adv. Synth. Catal., 2011, 353, 309.
22) “An Organogel Formed from a cyclic b-aminoalcohol”, C. Kang, Z. Bian, Y. He, F. Han, X. Qiu, L.-X. Gao, Chem. Commun., 2011, 47, 10746.
23) “Reliable and Diverse Synthesis of Aryl Azides via Copper-Catalyzed Coupling of Boronic Acids/Esters with TMSN3”, Y. Li, L. X. Gao, F. Han*, Chem. Eur. J., 2010, 16, 7969.
24) “Aryl Phosphoramides: Useful Electrophiles for Suzuki-Miyaura Coupling Catalyzed by NiCl2/dppp System”, Y. L. Zhao, Y. Li, Y. Li, L. X. Gao, F. Han*, Chem. Eur. J., 2010, 16, 4991.
25) “Luminescence Properties of Metallo-supramolecular Coordination Polymers Assembled from Pyridine Ring Functionalized Ditopic Bis-terpyridine and Ru(II) ions” F. Han, M. Higuchi, T. Ikeda, Y. Negishi, T. Tsukuda, D. G. Kurth, J. Mater. Chem., 2008, 18, 4555.
26) “Metallo-Supramolecular Polyelectrolytes Self-assembled from Various Pyridine Ring Substituted Bis-terpyridines and Metal Ions: Photophysical, Electrochemical and Electrochromic Properties” F. Han, M. Higuchi, D. G. Kurth, J. Am. Chem. Soc., 2008, 130, 2073.
27) “Metallo-Supramolecular Polymers Based on Functionalized Bis-terpyridines as Novel Electrochromic Materials” F. Han, M. Higuchi, D. G. Kurth, Adv. Mater., 2007, 19,3928.
28) “Design and Synthesis of Thiazoline-Thiazole Hybrid Macrocycles Possessing Strong Affinity to Pb2+ and Cd2+” F. Han, H. Tokuyama, T. Fukuyama, Chem. Comm., 2007, 3444.
29) “Novel Structural Motifs Consisting of Chiral Thiazolines: Synthesis, Molecular Recognition, and Anticancer Activity” F. Han, H. Osajima, M. Cheung, H. Tokuyama, and T. Fukuyama, Chem. Eur. J. 2007, 13,3026 (Selected as inside cover page).
30) “Diverse Synthesis of Novel Bisterpyridines via Suzuki-Type Cross-Coupling” F. Han, M. Higuchi, D. Kurth, Org. Lett., 2007, 9, 559-562.
31) “Synthesis of Chiral Cyclic Oligothiazolines: A Novel Structural Motif for a Macrocyclic Molecule”, F. Han, H. Osajima, M. Cheung, H. Tokuyama, and T. Fukuyama, Chem. Comm. 2006, 1757-1759.