2008年以前

 

2008

59. H. Liu, L. Wang,* P. Li, Highly Efficient and Recyclable Palladium Catalyst Anchored on Organic–Inorganic Hybrid Material: Application  in the Heck Reaction. Synthesis, 2008, 2405–2411. DOI: 10.1055/s-2008-1067161.

 

 

58. J. Yan, L. Wang,* Merrifield Resin Supported Dipeptides: Efficient and Recyclable Organocatalysts for Asymmetric Aldol Reactions under Neat Reaction Conditions. Synthesis, 2008, 2065–2072. DOI: 10.1055/s-2008-1067104.

 

 

57. J. Yan, L. Zhou, L. Wang,* Amination Reactions of Aryl Halides with Nitrogen-Containing Reagents Catalyzed by CuI in Ionic Liquid. Chin. J. Chem., 2008, 26, 165–169.

 

 

56. M. Wang, L. Wang,* Heterogeneous Palladium Chloride Catalyzed Ligand-free Suzuki-Miyaura Coupling Reactions at Ambient Temperature. Chin. J. Chem.,2008, 26, 1683–1688.

 

 

55. L. Zhang, L. Wang,* H. Li, P. Li, Application of Highly Efficient, Recyclable Organic-Inorganic Hybrid Material Immobilized Palladium Catalyst in Amine- and Phosphine-Free Suzuki-Miyaura Reaction. Synth. Commun., 2008, 38, 1498–1511.DOI: 10.1080/00397910801928509.

 

 

54. Q. Wu, L. Wang,* Immobilization of Copper(II) in Organic–Inorganic Hybrid Materials: A Highly Efficient and Reusable Catalyst for the Classic Ullmann Reaction. Synthesis, 2008, 2007–2012. DOI: 10.1055/s-2008-1067107.

 

 

52. L.-Y. Zhang, L. Wang,* Immobilized Palladium on Organic-inorganic Hybrid Materials: A Novel and Reusable Catalyst for the Copper-Free Sonogashira Coupling Reaction. Chin. J. Chem.,2008, 26, 1601–1606.

 

 

51. Z.-L. Wang, L.Wang,* J.-C. Yan, Palladium Immobilized on Silica Gel: A Novel and Reusable Catalyst for Heck Reaction. Chin. J. Chem., 2008, 26, 1721–1726.

 

 

50. T. Miao, L. Wang,* P. Li, J. Yan, A Highly Efficient and Recyclable Ionic Liquid Anchored Pyrrolidine Catalyst for Enantioselective Michael Additions. Synthesis, 2008, 3828–3834. DOI: 10.1055/s-0028-1083223.

 

 

49. T. Miao, L. Wang,* Regioselective Synthesis of 1,2,3-Triazoles by Use of a Silica-Supported Copper(I) Catalyst. Synthesis, 2008, 363–368. DOI: 10.1055/s-2008-1032037.

 

 

48. T. Miao, L. Wang,* Polystyrene-Immobilized Pyrrolidine as a Highly Stereoselectiveand Recyclable Organocatalyst for Asymmetric Michael Addition of Cyclohexanone to Nitroolefins. Tetrahedron Letters., 2008, 49, 2173–2176. DOI:10.1016/j.tetlet.2008.01.026.

 

 

47. P. Li, L. Wang,* M. Wang, F. You, Gold(I) Iodide Catalyzed Sonogashira Reactions. Eur. J. Org. Chem., 2008, 5946–5951. (Most Accessed Articles in 11/2008, Number 2 of Top 12). DOI: 10.1002/ejoc.200800765.

 

 

46. P. Li, L. Wang,* Y. Zhang, SiO2–NHC–Cu(I): an Efficient and Reusable Catalyst for [3+2] Cycloaddition of Organic Azides and Terminal Alkynes under Solvent-Free Reaction Conditions at Room Temperature. Tetrahedron, 2008, 64, 10825–10830. DOI:10.1016/j.tet.2008.09.021.

 

 

45. P. Li, L. Wang,* Y. Zhang, G. Wang, Silica gel Supported Pyrrolidine-Based Chiral Ionic Liquid as Recyclable Organocatalyst for Asymmetric Michael Addition to Nitrostyrenes. Tetrahedron, 2008, 64, 7633–7638. DOI:10.1016/j.tet.2008.05.039.

 

 

44. P. Li, L. Wang,* M. Wang, Y. Zhang, Pyrrolidine-Based Chiral Ionic Liquids as Recyclable Organocatalysts for Asymmetric Michael Additions to Nitrostyrenes under Solvent-Free Reaction Conditions. Eur. J. Org. Chem., 2008, 1157–1160. (Highlighted by: SYNFACTS2008, 5, 0548). DOI: 10.1002/ejoc.200701037.

 

 

43. P. Li, L. Wang,* Y. Zhang, M. Wang, Highly Efficient Three-Component (Aldehyde–Alkyne–Amine) Coupling Reactions Catalyzed by a Reusable PS-Supported NHC–Ag(I) under Solvent-Free Reaction Conditions. Tetrahedron Lett., 2008, 49, 6650–6654. (Highlighted by: SYNFACTS2009, 1, 0104). DOI:10.1016/j.tetlet.2008.09.026.

 

 

42. M. Wang, P. Li, L. Wang,* Silica-Immobilized NHC–CuI Complex: An Efficient and Reusable Catalyst for A3-Coupling (Aldehyde–Alkyne–Amine) under Solventless Reaction Conditions. Eur. J. Org. Chem., 2008, 2255–2261. (Highlighted by: SYNFACTS2008, 7, 0777). DOI: 10.1002/ejoc.200800006.

 

 

41. Z. Wang, L. Wang,* P. Li,Silica-Anchored Proline–Copper(I) as an Efficient and Recyclable Catalyst for the Sonogashira Reaction. Synthesis, 2008, 1367–1372. DOI: 10.1055/s-2008-1072562.

 

 

40. Y.-W. Dong , G.-W. Wang *, L. Wang,* Solvent-free synthesis of naphthopyrans under ball-milling conditions. Tetrahedron2008, 64, 10148–10154. DOI:10.1016/j.tet.2008.08.047.

 

 

39. G.-W. Wang*, Y.-B. Shen, X.-L. Wu, L. Wang,* Solvent-free hydroalkylation of olefins with 1,3-diketones catalyzed by phosphotungstic acid. Tetrahedron Letters2008, 49, 5090–5093. DOI:10.1016/j.tetlet.2008.06.029.

 

 

2007

38. L. Zhou, L. Wang,* Chiral Ionic Liquid Containing L-Proline Unit as a Highly Efficient and Recyclable Asymmetric Organocatalyst for Aldol Reaction. Chem. Lett.,2007, 36, 628–629.

 

 

37. P. Li, L. Wang,* A Highly Efficient Three-component Coupling of Aldehyde, Terminal Alkyne, and Amine via C-H Activation Catalyzed by Reusable Immobilized Copper in Organic–inorganic Hybrid Materials under Solvent-free Reaction Conditions. Tetrahedron, 2007, 63, 5455–5459. DOI:10.1016/j.tet.2007.04.032.

 

 

36. T. Miao, L. Wang,* Immobilization of Copper in Organic–inorganic Hybrid Materials: A Highly Efficient and Reusable Catalyst for the Ullmann Diaryl Etherification. Tetrahedron Lett., 2007, 48, 95–99. (Most Cited Paper 2006–2009 Award). DOI:10.1016/j.tetlet.2006.11.001.

 

 

35. H. Li, L. Wang,* P. Li, Application of Highly Efficient, Recyclable Organic–Inorganic Hybrid Material Immobilised Palladium Catalyst in Heck Reaction. Synthesis,2007, 1635–1642.DOI: 10.1055/s-2007-966065.

 

 

34. P. Li, L. Wang,* One-Pot Synthesis of 1,2,3-Triazoles from Benzyl and Alkyl Halides, Sodium Azide and Alkynes in Water Under Transition-Metal-Catalyst Free Reaction Conditions. Lett. Org. Chem., 2007, 4, 23–26.

 

 

2006

33. L. Zhang, L. Wang,* Silica-supported Copper(II) Catalyzed Coupling of Arylboronic Acids with Imidazoles. Chin. J. Chem.2006, 24(11),1605–1608.

 

 

32. L. Wang,* P. Li, Recoverable Palladium(0) on Poly(vinylpyrrolidone) Catalyzed Ligand-free Suzuki Reaction in Water. Chin. J. Chem.2006, 24, 770–774.

 

 

31. P. Li, L. Wang,* An Amine-, Copper- and Phosphine-free Sonogashira Coupling Reaction Catalyzed by Immobilization of Palladium in Organic–inorganic Hybrid Materials. Adv. Synth. Catal., 2006,348, 681–685. DOI: 10.1002/adsc.200505343.

 

 

30. P. Li, L. Wang,* A Novel Silver Iodide Catalyzed Sonogashira Coupling Reaction. Synlett, 2006, 2261–2265. DOI: 10.1055/s-2006-949640.

 

 

29. H. Li, L. Wang,* Triethanolamine as an Efficient and Reusable Base, Ligand and Reaction Medium for Phosphine-free Palladium Catalyzed Heck Reaction. Eur. J. Org. Chem., 2006, 5099–5102. DOI: 10.1002/ejoc.200600561.

 

 

28. E. You, P. Li, L. Wang,* Nickel(0)/Tetra-n-butylammonium Bromide (TBAB) Catalyzed Suzuki-Miyaura Reaction. Synthesis,2006, 1465–1469.DOI: 10.1055/s-2006-926424.

 

 

27. L. Zhou, L. Wang,* Functionalized Ionic Liquid as an Efficient and Recyclable Reaction Medium for Phosphine-free Palladium Catalyzed Heck Reaction. Synthesis,2006, 2653–2658.DOI: 10.1055/s-2006-942466.

 

 

26. L. Zhang, P. Li, L. Wang,* A Silica-Supported Copper(I) Catalyzed Sonogashira Coupling Reaction. Lett. Org. Chem., 2006, 3, 282–285.

 

 

25. E. You, L. Wang,* A Novel Cu(II) Catalyzed Sonogashira Reaction. J. Chem. Res., 2006, 555–557.

 

 

2005

24. P. Li, L. Wang,* Mercuous Chloride Catalyzed Mannich Condensation of Terminal Alkynes with Secondary Amines and Aldehydes. Chin. J. Chem.2005, 23(8), 1076–1080.

 

 

23. P. Li, L. Wang,* H. Li, Application of Recoverable Nanosized Palladium(0) Catalyst in Sonogashira Reaction. Tetrahedron, 2005, 61, 8633–8640. DOI:10.1016/j.tet.2005.07.013.

 

 

22. L. Wang,* M. Wang, F. Huang, A Simple Copper Salt-Catalyzed Synthesis of Unsymmetrical Diaryl Selenides and Tellurides from Arylboronic Acids with Diphenyl Diselenide and Ditelluride. Synlett, 2005, 2007–2010. DOI: 10.1055/s-2005-871936.

 

 

21. L. Wang,* J. Yan, P. Li, M. Wang, C. Su, The Effects of Amines on Oxidative Homo-coupling of Terminal Alkynes Promoted by Copper Salt. Tuning of Reactivity towards Glaser or Sonogashira Coupling Depending on the Reaction Medium. J. Chem. Res., 2005, (2), 112–115.

 

 

 

20. J. Yan, L. Wang,* First Example of Transition-Metal-Free Glaser-Type Coupling Reaction. Synth. Commun., 2005, 35, 2333–2338. DOI: 10.1080/00397910500187191.

 

 

2004

19. P. Li, W. Rao, M. Wang and L. Wang,* Ultrasonic-Enhanced Stereoselective Debromination of vic-Dibromides to Alkenes with Metallic Zinc Powder in Aqueous Media. Chem. Res. Chin. Univ.2004, 20(5), 598–601. Article ID: 100529040 (2004) 2052598204.

 

 

18. M. Wang, L. Wang,* P. Li, J. Yan, A Novel Debromination of vic-Dibromides to Alkenes with InCl3(cat.)/Sm System in Aqueous Media. Chin. J. Chem. 2004, 22(8), 863–866.

 

 

17. P. Li, L. Wang,* M. Wang, J. Yan, Nickel Chloride Promoted Glaser Coupling Reaction in Hot Water. Chin. Chem. Lett.2004, 15(11), 1295–1298.

 

 

16. P. Li, J. Tan, M. Wang, L, Wang,* Glaser Coupling Reaction without Organic Solvents and Bases under Near-critical Water Conditions. Chin. J. Chem.2004, 22(2), 219–221.

 

 

15. L. Wang,* P. Li, Y. Zhang, The Sonogashira Coupling Reaction Catalyzed by Ultrafine Nickel(0) Powder. Chem. Commun., 2004, 514–515. (Most Accessed Articles in 2/2004, Top 10). DOI: 10.1039/b314246a.

 

 

14. J. Yan, Z. Wang, L. Wang,* Microwave-accelerated Solventless Sonogashira-like Coupling Reaction of 1,1-Dibromo-1-alkenes with Organic Halides on Nickel(0) Powder-doped KF/Al2O3. J. Chem. Res., 2004, 71–73.

 

 

13. P. Li, L. Wang,* Y. Yang, X. Sun, M. Wang, J. Yan, A Novel Reduction of Sodium Alkyl Thiosulfates with InCl3(cat.)/Sm(0) System in Aqueous Media: Facile Synthesis of Disulfides. Heteroatom Chem., 2004, 15, 376–379. DOI 10.1002/hc.20023.

 

 

12. M. Wang, P. Li, L. Wang,* Microwave Irradiated Solventless Sonogashira Reaction on Nickel(0) Powder Doped KF/Al2O3. Synth. Commun., 2004, 34, 2803–2812. DOI: 10.1081/SCC-200026232.

 

 

2003

11. L. Wang,* P. Li, Y. Chen, J. Yan, M. Wang, A Convenient and Rapid Microwave-Enhanced, Solventless Desilylation Procedure Using Potassium Carbonate Doped Silica Gel. Chin. J. Org. Chem. 2003, 23, 720–723.

 

 

10.     Lei Wang,* P. Li, J. Yan, J. Chen, Reduction of Azides to Amines with Zinc Metal in Near-Critical Water (NCW). Chem. J. Inter. 2003, 5, 25–29.

 

 

9. L. Wang,* P. Li, Microwave-Enhanced Mannich Condensation of Terminal Alkynes, Primary Amines with Paraformaldehyde on Cuprous Iodide Doped Alumina under Solvent Free Conditions. Chin. J. Chem. 2003, 21, 710–713.

 

 

8. L. Wang,* P. Li, Sonogashira Coupling Reaction with Palladium Powder, Potassium Fluoride in Methanol. Chin. J. Chem.2003, 21, 474–476.

 

 

7. L. Wang,* P. Li, Z. Jiang, Preparation of Aromatic Amines by Reduction of Aromatic Nitro Compounds with Metallic Tellurium in Near-Critical Water. Chin. J. Chem. 2003, 21, 222–224.

 

 

6. L. Wang,* P. Li, J. Yan, Z. Wu, A Novel Preparation of Methyl Ketones through One-Carbon Homologation of Aldehydes. Tetrahedron Lett., 2003, 44, 4685–4687. DOI: 10.1016/S0040-4039(03)01084-0.

 

 

5. L. Wang,* P. Li, Z. Wu, J. Yan, M. Wang, Reduction of Aromatic Nitro Compounds to Aromatic Amines with Nano-sized Activated Metallic Iron Powder in Water. Synthesis,2003, 20012004.DOI: 10.1055/s-2003-41021.

 

 

4. L. Wang,* P. Li, Y. Xie, Y. Ding, Unexpected Chemoselective Debromination and Hydrogenation of 1,1-Dibromo-1-alkenes Mediated by Samarium Metal in Methanol. Synlett, 2003, 1137–1140. ISSN: 1234-567-89.

 

 

3. L. Wang,* P. Li, Sonogashira Coupling Reaction with Palladium Powder, Potassium Fluoride in Aqueous Media. Synth. Commun., 2003, 33, 3679–3685. DOI: 10.1081/SCC-120025176.

 

 

2. L. Wang,* P. Li, J. Chen, J. Yan, Novel Reduction of Azides to Amines with Tellurium Metal in Near-Critical Water. Phosphorus, Sulfur, and Silicon, 2003, 178, 1807–1813. DOI: 10.1080/10426500390221465.

 

 

2002

1. L. Wang,* P. Li, L. Zhou, A Novel Reduction of Sodium Alkyl Thiosulfates Using Samarium Metal without Activating Agent in Water. Tetrahedron Lett., 2002, 43, 8141–8143. PII: S0040-4039(02)01915-9.