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    The current position: Organic Chemistry
Cheng Ying

Published Date： 2016-02-28

Cheng Ying

Cheng Ying 中文

 

 

 

Representative papers

  1. N-Heterocyclic Carbene-catalyzed Cascade Annulation Reaction of o-Vinylarylaldehydes with Nitrosoarenes: One-Step Assembly of Functionalized 2,3-Benzoxazin-4-ones”
  2. Zhong-Xin Sun and Ying Cheng*, Org. Biomol. Chem., 2012, 10 (20), 4088-4094.
  3. The Reaction of beta-Lactam Carbenes with 3,6-Dipyridyltetrazines: Switch of Reaction Pathways by 2-Pyridyl and 4-Pyridyl Substituents of Tetrazines”
  4. Xiao-Rong Wang, Juan Xing, Cai-Xia Yan  and Ying Cheng*, Org. Biomol. Chem., 2012, 10 (5), 970-977.
  5. “Construction of Novel Tricyclic Fused-ring Systems by the Multicomponent Reactions of Imidazo[1,5-a]pyridine Carbenes with Ortho Aromatic Dialdehydes and Electron-deficient Alkynes”Cai-Xia Yan, Zhong-Xin Sun and Ying Cheng*, Synthesis, 2012, 44, 865-874.
  6. “The Nucleophilic Addition of b-Lactam Carbenes to AlkylphenylKetenes for a Ready Approach to Spiro[b-lactam-2,1'-indene] Derivatives”Yong-Jia Li, Cai-Xia Yan, Zhong-Xin Sun and Ying Cheng*, Aust. J. Chem. 2012, 65, 417-426.
  7. “Reaction of b-Lactam Carbenes with 2-Pyridyl Isonitriles: a One-pot Synthesis of 2-Carbonyl-3-(pyridylamino)imidazo[1,2-a]pyridines Useful as Fluorescent Probes for Mercury Ion”Na Shao, Guang-Xian Pang, Cai-Xia Yan, Gao-Feng Shi, and Ying Cheng*, J. Org. Chem. 2011, 76(18), 7458-7465.
  8. “Interaction of β-Lactam Carbenes with 3,6-Diphenyltetrazines:A Five-Step Cascade Reaction for the Direct Construction of Indeno[2,1-b]pyrrol-2-ones”Juan Xing, Xiao-Rong Wang, Cai-Xia Yan, and Ying Cheng*, J. Org. Chem. 2011, 76(11), 4746-4752.
  9.  “N-Heterocyclic Carbene-catalyzed Reaction of Phthalaldehydes: Controllable Stereoselective Synthesis of Polyhydroxylated Spiro- and Fused Indenones Dictated by the Structure of NHC Catalysts”
  10. Ying Cheng*, Jiang-Hua Peng, Yong-Jia Li, Xun-Yu Shi, Ming-Sheng Tang, Tian-Yu Tan, J. Org. Chem., 2011, 76(6), 1844-1851.
  11. “The Multicomponent Reaction of Imidazo[1,5-a]pyridine Carbenes with Phthalaldehydes and Dimethyl Acetylenedicarboxylate: a Facile Construction of Benzo[d]furo[3,2-b]azepines and Their Photophysical Properties”
  12. Huan-Rui Pan, Xiao-Rong Wang, Cai-Xia Yan, Zhong-Xin Sun, Ying Cheng*, Org. Biomol. Chem., 2011, 9, 2166-2174.
  13. “Multicomponent Reaction of Imidazo[1,5-a]pyridine Carbenes with Aldehydes and Dimethyl Acetylenedicarboxylate or Allenoates: A Straightforward Approach to Fully Substituted Furans”Huan-Rui Pan, Yong-Jia Li, Cai-Xia Yan, Juan Xing, and Ying Cheng,* J. Org. Chem., 2010, 75 (19), 6644-6652.
  14. “Orthogonal Synthesis of Densely Functionalized Pyrroles and Thiophenes
  15. from the Reactions of Imidazo[1,5-a]pyridine Carbene-Derived Zwitterions with Electron-Deficient Alkynes”
  16. Ying Cheng,* Jiang-Hua Peng, and Jia-Qi Li, J. Org. Chem., 2010, 75 (7), 2382-2388.
  17. “Dimerization of 2-Pyridylisonitriles Produces p-Extended Fused Heteroarenes Useful as Highly Selective Colorimetric and Optical Probes for Copper Ion”Na Shao, Guang-Xian Pang, Xiao-Rong Wang, Rui-Juan Wu, Ying Cheng*, Tetrahedron, 2010, 66 (36), 7302-7308.
  18.  “Synthesis of Novel and Versatile Synthetic Intermediates from the Reaction of Benzoimidazole and Triazole Carbenes with Ketenimines and their Application in the Construction of Spiro-pyrroles”Jun-Ming Mo, Yang-Guang Ma and Ying Cheng*, Org. Biomol. Chem., 2009, 7(23), 5010-5019.
  19.  “The [3+2] Cycloaddition Reaction of Thiazole Carbene-derived C-C-Se 1,3-Dipoles: a Concise and Highly Efficient Strategy for the Construction of Multifunctional Dihydroselenophenes and Selenopheno[2,3-b]pyrazines”Jian-Hong Zhang and Ying Cheng *, Org. Biomol. Chem., 2009, 7(16), 3264-3270.
  20. “An Experimental and Theoretical Study on the Interaction of N-Heterocyclic Carbene-Derived 1,3-Dipoles with Methoxycarbonylallenes: Highly Regio- and Stereoselective [3+2]-Cycloadditions Controlled by the Structures of N-Heterocycles of 1,3-Dipoles”Ying Cheng*, Bo Wang, Xiao-Rong Wang, Jian-Hong Zhang and De-Cai Fang*, J. Org. Chem., 2009, 74 (6), 2357-2367.
  21. “An Unprecedented Chemospecific and Stereoselective Tandem Nucleophilic Addition/Cycloaddition Reaction of Nucleophilic Carbenes with Ketenimines”   Ying Cheng*, Yang-Guang Ma, Xiao-Rong Wang and Jun-Ming Mo; J. Org. Chem., 2009, 74 (2), 850-855.
  22. “A Concise Synthesis of Benzo[h]-?and Pyrido[3,2-h]-d-carbolin-2,4-diones from One-pot Reaction of b-Lactam Carbenes with Naphthyl- and Quinolyl Isonitriles” Gao-Feng Shi, Zhi-Mei Kang, Xiao-Ping Jiang, and Ying Cheng*, Synthesis, 2008, (18), 2883-2980.
  23.  “Solvent Controlled Divergent Syntheses of Polysubstituted Pyrroles and Pyrrolo[2,3-b]-1,4-thiazines”Ying Cheng *, Zhi-Mei Kang, Yang-Guang Ma, Jiang-Hua Peng, Mei-Fang Liu; Tetrahedron, 2008, 64 (30-31), 7362-7368.
  24. “Concise and Divergent Total Synthesis of Swainsonine, 7-Alkylswainsonines and 2,8a-Diepilentiginosine via a Chiral Heterocyclic Enaminoester Intermediate”Gao-Feng Shi, Jia-Qi Li, Xiao-Ping Jiang and Ying Cheng*, Tetrahedron, 2008, 64, 5005-5012.
  25.  “Highly Site, Regio- and Stereoselective Multicomponent Reaction of Benzimidazole Carbenes, Isothiocyanates and Allenoates”
  26. Bo Wang, Jia-Qi Li, Ying Cheng*, Tetrahedron Lett., 2008, 49, 485-489.
  27. “The unprecedented ring transformation from thiazoline-spiro-thiophene to thieno[2,3-b]pyrazine involved in the reaction of 2-thiocarbamoyl thiazolium salts with dimethyl acetylenedicarboxylate”Yang-Guang Ma and Ying Cheng*, Chem. Commun., 2007, (47), 5087-5089.
  28. “Substrate Controlled and Site Selective [3+2]-Cycloadditions of N-Heterocyclic Carbene Derived Ambident Dipoles”
  29. Ying Cheng*, Mei-Fang Liu, De-Cai Fang* and Xue-Mei Lei, Chem. Eur. J., 2007, 13 (15), 4282-4292.
  30. “Highly Efficient and Site Selective [3+2] Cycloaddition of Carbene-Derived Ambident Dipoles with Ketenes for a Straightforward Synthesis of Spiro-pyrrolidones”
  31. Jia-Qi Li, Rong-Zhen Liao, Wan-Jian Ding, and Ying Cheng*, J. Org. Chem., 2007, 72, 6266-6269.
  32.  “The Interaction of b-Lactam Carbenes with Aryl Isonitriles: an Unprecedented Rearrangement of 2-Azetidinonylidene Indoles to d-Carbolinones”  
  33. Ying Cheng* and Lan-Qing Cheng, J. Org. Chem., 2007, 72 (7), 2625-2630.
  34.  “A Versatile Strategy for Divergent and Diastereoselective Synthesis of Natural Product-Like Polyhydroxylated Indolizidines”
  35. Xiao-Ping Jiang, Ying Cheng*, Gao-Feng Shi, and Zhi-Mei Kang, J. Org. Chem., 2007, 72 (6), 2212-2215.
  36. “Reaction of b-lactam carbenes with alkyl isonitriles for a ready approach to 4-cyano and 4-carbamoyl substituted b-lactams
  37. Lan-Qing Cheng and Ying Cheng*, Tetrahedron, 2007, 63(38), 9359-9364.
  38.  “An Unprecedented Tandem 1,3-Dipolar Cycloaddition/Cheletropic Elimination: a Facial Approach to Novel Push-Pull Olefins”
  39. Qing Zhu, Mei-Fang Liu, Bo Wang and Ying Cheng*, Org. Biomol. Chem., 2007, 5, 1282-1286.
  40. “A N-heterocyclic carbene derived highly regioselective ambident C-C-S and C-C-N 1,3-dipolar system”Mei-Fang Liu, Bo Wang and Ying Cheng*, Chem. Commun., 2006, (11), 1215-1217.
  41. “High Nucleophilicity of Cyclic Amidocarbene toward Aryl Isocyanates, New Approach to Spiro[azetidinone-4,3’-indolinone] Derivatives”Ying Cheng*, Bo Wang, and Lan-Qing Cheng, J. Org. Chem., 2006, 71(12), 4418-4427.
  42. “The Interaction of Aryloxychlorocarbenes with Acetylenedicarboxylate: Novel Formation of Polyfunctional Butadienes and 8-Oxatricyclo[3.2.1.02.4]oct-6-enes”Ying Cheng*, Qing Zhu, Quan Song Li, and Otto Meth-Cohn, J. Org. Chem., 2005, 70 (12), 4840-4846.
  43. “Heterocycles derived from heteroatom-substituted carbenes”Ying Cheng* and Otto Meth-Cohn*, Chem. Rev., 2004, 104 (5), 2507-2530.
  44.  “Heterocyclic Enamines: the Versatile Intermediates in the Synthesis of Heterocyclic Compounds and Natural Products”Ying Cheng*, Zhi-Tang Huang and Mei-Xiang Wang*, Current Org. Chem., 2004, 8 (4), 325-350.
  45.  “A Simple One-Pot reaction to the Bis-dibenzo[b,f][1,5]diazocines: The Useful Precursors of Novel Macrocycles”Ying Cheng*, Bo Wang, Otto Meth-Cohn, Synthesis, 2003, 18, 2839-2843.
  46. “The surprising nucleophilic addition of aminochlorocarbenes to diethylacetylenedicarboxylate and to oxalyl chloride: Quinolines and benzo[1,4]diazepines from N-alkylformanilides and oxalyl chloride in the presence of Hunig’s base”Ying Cheng*, Hua Yang and Otto Meth-Cohn*, Org. Biomol. Chem., 2003, 1 (20), 3605-3610.
  47. “The unique nucleophilic reactivity of arylaminochlorcarbenes”Ying Cheng*, Hua Yang, Otto Meth-Cohn*, Chem. Commun., 2003, 90-91.
  48. “Synthetic applications of aminochlorocarbenes: a two-step conversion of N-methylformanilides into 3-arylamino-2-chloroindoles”Ying Cheng*, Yu-Hua Zhan, Hai-Xia Guan, Otto Meth-Cohn*, Synthesis, 2002, 16, 2426-2430.
  49.  “Unexpected ring size effect of the annulation of heterocyclic secondary enamines with dicarboxylic acid dichloridesYing Cheng*, Hai-Bo Yang, Mei-Xiang Wang*, Davia J. Williams, Tetrahedron, 2002, 58, 2821-2829.
  50. “A simple route to N-w-chloroalkylisatins from cyclic t-anilines, oxalyl chloride and DABCO”Ying Cheng*, Yu-Hua Zhan, Otto Meth-Cohn*, Synthesis, 2002, 1, 34-38.
  51. “A very simple route to benzonaphtho[1,5]diazocines using Vilsmeier reagents via the t-amino effect”Ying Cheng*, Hai-Bo Yang, Bo Liu, Otto Meth-Cohn*, David Watkin, Stephen Humphries, Synthesis, 2002, 7, 906-910.
  52. “Annulation of heterocyclic secondary enamines with dicarboxylic acid dichlorides, an unexpected ring size effect”Ying Cheng*, Hai-Bo Yang, Zhi-Tang Huang, Mei-Xiang Wang*, Tetrahedron Lett., 2001, 42, 1757-1759.
  53. “A very simple route to methylisatins: Friedel-Crafts acylation of p-substituted N,N-dimethylanilines with oxalyl chloride and DABCO”Ying Cheng*, Hai-Lin Ye, Yu-Hua Zhan, Otto Meth-Cohn*, Synthesis, 2001, 6, 904-908.
  54. “Unexpected products from formylation of N,N-dimethylanilines with 2-formamidopyridine in POCl3”Ying Cheng*, Peng Jiao, Davia J. Williams, Otto Meth-Cohn*, J.C.S. Perkin Trans 1, 2001, 44-46.
  55. “En route to Molecular Bracelets: The synthesis of linear pentacyclic bis-(benzodiazocino)benzenes.”Ying Cheng*, Qing-Xiang Liu and Otto Meth-Cohn*, Synthesis, 2000, 640-642.
  56.  “Surprising formylations with methylformamidopyridines and oxalyl chloride.”Ying Cheng*, Qing-Xiang Liu and Otto Meth-Cohn*, Tetrahedron Lett., 2000, 41, 3475-3478.
  57. “Vilsmeier formalytion of tert-anilines: dibenzo[b,f][1,5]diazocines and quinazolinium salts via the t-amino effect.”Ying Cheng, Otto Meth-Cohn* and David Taylor, J. C. S., Perkin Trans.1, 1998, 1257-1262.
  58. “Umpoled Vilsmeier reagents. The chemistry of aminochlorocarbenes derived from Vilsmeier reagents by the action of bases.”Ying Cheng, Simon Goon and Otto Meth-Cohn*, J. C. S., Perkin Trans.1, 1998, 1619-1625.
  59. “Carbenes from Vilsmeier reagents by the action of bases in POCl3; the umpolung of Vilsmeier reagents”.Ying Cheng, Simon Goon and Otto Meth-Cohn*, Chem. Commun., 1996, 1395-1396.
  60. The Vilsmeier Formylation of N-(4-Tolyl)pyrrolidine, -piperidine and -perhydroazepine: Further Examples of the t-Amino Effect”
  61. Otto Meth-Cohn* and Ying Cheng, Tetrahedron Lett. 1996, 37, 2679-2682.

 
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