Citation: Li Xiaojun, Zhang Wanbin, Gao Shuanhu. Total Synthesis of Complex Natural Products: Combination of Chemical Synthesis and Biosynthesis Strategies[J]. Chinese Journal of Organic Chemistry, ;2018, 38(9): 2185-2198. doi: 10.6023/cjoc201806019 shu

Total Synthesis of Complex Natural Products: Combination of Chemical Synthesis and Biosynthesis Strategies

  • Corresponding author: Zhang Wanbin, wanbin@sjtu.edu.cn Gao Shuanhu, shgao@chem.ecnu.edu.cn
  • Received Date: 14 June 2018
    Revised Date: 9 July 2018
    Available Online: 16 September 2018

    Fund Project: Project supported by the National Natural Science Foundation of China (No. 21772044), the National Young Top-Notch Talent Support Program of Shanghai Academic/Technology Research Leader (No. 18XD1401500) and the Fundamental Research Funds for the Central Universitiesthe National Young Top-Notch Talent Support Program of Shanghai Academic/Technology Research Leader 18XD1401500the National Natural Science Foundation of China 21772044

Figures(18)

  • Total synthesis of natural products is one of the most important field in organic chemistry. Natural products and derivatives, containing complex structures and potential biological activities, are also indispensable sources of drug discovery. The total synthesis of natural products through the combination of chemical synthesis and biosynthesis strategies is reviewed. The main content includes the chemical and biosynthetic studies of artemisinin, spinosyn A, myceliothernophin E and equisetin.
  • 加载中
    1. [1]

      Newman, D. J.; Cragg, G. M. J. Nat. Prod. 2016, 79, 629.  doi: 10.1021/acs.jnatprod.5b01055

    2. [2]

      Wöhler, F.; Ueber K. B.; Des, H. Ann. Phys. 1828, 88, 253.  doi: 10.1002/(ISSN)1521-3889

    3. [3]

      (a) Nicolaou, K. C.; Vourloumis, D.; Winssinger, N.; Baran, P. S. Angew. Chem., Int. Ed. 2000, 39, 44.
      (b) Nicolaou, K. C. J. Org. Chem. 2009, 74, 951.
      (c) Hoffmann, R. W. Angew. Chem., Int. Ed. 2013, 52, 123.
      (d) Keasling, J. D.; Mendoza, A.; Baran, P. S. Nature 2012, 492, 188.

    4. [4]

      (a) Aicher, T. D.; Buszek, K. R.; Fang, F. G.; Forsyth, C. J.; Jung, S. H.; Kishi, Y.; Matelich, M. C.; Scola, P. M.; Spero, D. M.; Yoon, S. K. J. Am. Chem. Soc. 1992, 114, 3162.
      (b) Duan, J. J.-W.; Kishi, Y. Tetrahedron Lett. 1993, 34, 7541.
      (c) Stamos, D. P.; Kishi, Y. Tetrahedron Lett. 1996, 37, 8643.
      (d) Stamos, D. P.; Sean, S. C.; Kishi, Y. J. Org. Chem. 1997, 62, 7552.
      (e) Namba, K.; Kishi, Y. J. Am. Chem. Soc. 2005, 127, 15382.
      (f) Dong, C.-G.; Henderson, J. A.; Kaburagi, Y.; Sasaki, T.; Kim, D.-S.; Kim, J. T.; Urabe, D.; Guo, H.; Kishi, Y. J. Am. Chem. Soc. 2009, 131, 15642.
      (g) Yang, Y.-R.; Kim, D.-S.; Kishi, Y. Org. Lett. 2009, 20, 4516.
      (h) Liu, L.; Henderson, J. A.; Yamamoto, A.; Bremond, P.; Kishi, Y. Org. Lett. 2012, 14, 2262.
      (i) Shan, M.; Kishi, Y. Org. Lett. 2012, 14, 660.
      (j) Lee, J. H.; Li, Z.; Osawa, A.; Kishi, Y. J. Am. Chem. Soc. 2016, 138, 16248.

    5. [5]

      (a) Kingston, D. G. Phytochemistry 2007, 68, 1844.
      (b) Wani, M. C.; Taylor, H. L.; Wall, M. E.; Coggon, P.; McPhail, A. T. J. Am. Chem. Soc. 1971, 93, 2325.

    6. [6]

      Ajikumar, P. K.; Xiao, W.-H.; Tyo, K. E. J.; Wang, Y.; Simeon, F.; Leonard, E.; Mucha, O.; Phon, T. H.; Pfeifer, B.; Stephanopoulo, G. Science 2010, 330, 70.  doi: 10.1126/science.1191652

    7. [7]

      (a) World Health Organization 18th WHO Essential Medicines List, Geneva, Switzerland, 2013.
      (b) Seya, M. J.; Gelders, S. F.; Achara, O. U.; Milani, B.; Scholten, W. K. J. Pain Palliat. Care Pharmacother. 2011, 25, 6.
      (c) International Narcotics Control Board (INCB) Narcotic Drugs: Estimated World Requirements for 2015——Statistics for 2013, New York, 2014.

    8. [8]

      Galanie, S.; Thodey, K.; Trenchard, I. J.; Interrante, M. F.; Smolke, C. D. Science 2015, 349, 1095.  doi: 10.1126/science.aac9373

    9. [9]

      Klayman, D. L. Science 1985, 228, 104.

    10. [10]

      Davies, E. E. Ann. Trop. Med. Parasitol. 1975, 69, 147-154.  doi: 10.1080/00034983.1975.11686996

    11. [11]

      Theakston, R. D. G. Life Sci. 1969, 8, 521-529.  doi: 10.1016/0024-3205(69)90251-3

    12. [12]

      Liu, C. C.; Wang, Y. C.; Ouyang, F. Prog. Chem. 1999, 11, 41.  doi: 10.3321/j.issn:1005-281X.1999.01.006

    13. [13]

    14. [14]

      (a) Schmid, G.; Hofheinz, W. J. Am. Chem. Soc. 1983, 105, 624.
      (b) Yadav, J. S.; Babu, R. S.; Sabitha, G. Tetrahedron Lett. 2003, 44, 387.
      (c) Yadav, J. S.; Thirupathaiah, B.; Srihari, P. Tetrahedron 2010, 66, 2005.
      (d) Zhu, C.; Cook, S. P. J. Am. Chem. Soc. 2012, 134, 13577.

    15. [15]

    16. [16]

    17. [17]

      Liu, D.; Zhang, W. Chin. Sci. Bull. 2017, 62, 1997(in Chinese).
       

    18. [18]

    19. [19]

      (a) Martin, V. J. J.; Pitera, D. J.; Withers, S. T.; Newman, J. D.; Keasling, J. D. Nat. Biotechnol. 2003, 21, 796.
      (b) Brown, G. D. Molecules 2010, 15, 7603.
      (c) Tsuruta, H.; Paddon, C. J.; Eng, D.; Lenihan, J. R.; Horning, T.; Anthony, L. C.; Regentin, R.; Keasling, J. D.; Renninger, N. S.; Newman, J. D. PLoS One 2009, 4, e4489.
      (d) Ro, D.-K.; Paradise, E. M.; Ouellet, M.; Fisher, K. J.; Newman, K. L.; Ndungu, J. M.; Ho, K. A.; Eachus, R. A.; Ham, T. S.; Kirby, J.; Chang, M. C. Y.; Withers, S. T.; Shiba, Y.; Sarpong, R.; Keasling, J. D. Nature 2006, 440, 940.
      (e) Westfall, P. J.; Pitera, D. J.; Lenihan, J. R.; Eng, D.; Woolard, F. X.; Regentin, R.; Horning, T.; Tsuruta, H.; Melis, D. J.; Owens, A.; Fickes, S.; Diola, D.; Benjamin, K. R.; Keasling, J. D.; Leavell, M. D.; McPhee, D. J.; Renninger, N. S.; Newman, J. D.; Paddon, C. J. Proc. Natl. Acad. Sci. U. S. A. 2012, 109, E111.
      (f) Bouwmeester, H. J.; Wallaart, T. E.; Janssen, M. H. A.; Loo, B. V.; Jansen, B. J. M.; Posthumus, M. A.; Schmidt, C. O.; De Kraker, J.-W.; Kö nig, W. A.; Franssen, M. C. R. Phytochemistry 1999, 52, 843.
      (g) Mercke, P.; Bengtsson, M.; Bouwmeester, H. J.; Posthumus, M. A.; Brodelius, P. E. Arch. Biochem. Biophys. 2000, 381, 173.
      (h) Teoh, K. H.; Polichuk, D. R.; Reed, D. W.; Covello, P. S. Botany 2009, 87, 635.
      (i) Paddon, C. J.; Westfall, P. J.; Pitera, D. J.; Benjamin, K.; Fisher, K.; McPhee, D.; Leavell, M. D.; Tai, A.; Main, A.; Eng, D.; Polichuk, D. R.; Teoh, K. H.; Reed, D. W.; Treynor, T.; Lenihan, J.; Jiang, H.; Fleck, M.; Bajad, S.; Dang, G.; Dengrove, D.; Diola, D.; Dorin, G.; Ellens, K. W.; Fickes, S.; Galazzo, J.; Gaucher, S. P.; Geistlinger, T.; Henry, R.; Hepp, M.; Horning, T.; Iqbal, T.; Kizer, L.; Lieu, B.; Melis, D.; Moss, N.; Regentin, R.; Secrest, S.; Tsuruta, H.; Vazquez, R.; Westblade, L. F.; Xu, L.; Yu, M.; Zhang, Y.; Zhao, L.; Lievense, J.; Covello, P. S.; Keasling, J. D.; Reiling, K. K.; Renninger, N. S.; Newman, J. D. Nature 2013, 496, 528.

    20. [20]

      (a) Acton, N.; Roth, R. J. J. Nat. Prod. 1989, 52, 1183.
      (b) Acton, N.; Roth, R. J. J. Org. Chem. 1992, 57, 3610.
      (c) Haynes, R. K.; Vonwiller, S. C. J. Chem. Soc., Chem. Commun. 1990, 451.
      (d) Sy, L.-K.; Brown, G. D. Tetrahedron 2002, 58, 897.

    21. [21]

      (a) Zhang, W.; Liu, D.; Yuan, Q. CN 102718773, 2012.
      (b) Li, J.; Shen, J.; Xia, C.; Wang, Y.; Liu, D.; Zhang, W. Org. Lett. 2016, 18, 2122.

    22. [22]

      (a) Sparks, T. C.; Crouse, G. D.; Durst, G. Pest Manage. Sci. 2001, 57, 896.
      (b) Kirst, H. A. J. Antibiot. 2010, 63, 101.
      (c) Kirst, H. A.; Michel, K. H.; Martin, J. W.; Creemer, L. C.; Chio, E. H.; Yao, R. C.; Nakatsukasa, W. M.; Boeck, L. D.; Occolowitz, J. L.; Paschal, J. W.; Deeter, J. B.; Jones, N. D.; Thompson, G. D. Tetrahedron Lett. 1991, 32, 4839.

    23. [23]

      Evans, D. A.; Black, W. C. J. Am. Chem. Soc. 1993, 115, 4497.  doi: 10.1021/ja00064a011

    24. [24]

      (a) Evans, D. A.; Bartroli, J.; Shih, T. L. J. Am. Chem. Soc. 1981, 103, 2127.
      (b) Evans, D. A.; Gage, J. R. Org. Synth. 1989, 68, 83.

    25. [25]

      (a) Hikota, M.; Tone, H.; Horita, K.; Yonemitsu, O. J. Org. Chem. 1990, 55, 7.
      (b) Inanaga, J.; Hirata, K.; Saeki, H.; Katsuki, T.; Yamaguchi, M. Bull. Chem. Soc. Jpn. 1979, 52, 1989.

    26. [26]

      (a) Stille, J. K.; Groh, B. L. J. Am. Chem. Soc. 1987, 109, 813.
      (b) Stille, J. K.; Sweet, M. P. Tetrahedron Lett. 1989, 30, 3645.

    27. [27]

      Evans, D. A.; Chapman, K. T.; Bisaha, J. J. Am. Chem. Soc. 1988, 110, 1238.  doi: 10.1021/ja00212a037

    28. [28]

      (a) Paquette, L. A.; Gao, Z.; Ni, Z.; Smith, G. F. J. Am. Chem. Soc. 1998, 120, 2543.
      (b) Paquette, L. A.; Collado, I.; Purdie, M. J. Am. Chem. Soc. 1998, 120, 2553.

    29. [29]

      (a) Mukaiyama, T.; Kobayashi, S.; Shoda, S.-I. Chem. Lett. 1984, 907.
      (b) Evans, D. A.; Kaldor, S. W.; Jones, T. K.; Clardy, J.; Stout, T. J. J. Am. Chem. Soc. 1990, 112, 7001.

    30. [30]

      (a) Mergott, D. J.; Frank, S. A.; Roush, W. R. Proc. Natl. Acad. Sci. U. S. A. 2004, 101, 11955.
      (b) Winbush, S. M.; Mergott, D. J.; Roush, W. R. J. Org. Chem. 2008, 73, 1818.

    31. [31]

      (a) Boeckman, R. K. Jr.; Barta, T. E. J. Org. Chem. 1985, 50, 3421.
      (b) Roush, W. R.; Kageyama, M. Tetrahedron Lett. 1985, 26, 4327.
      (c) Roush, W. R.; Kageyama, M.; Riva, R.; Brown, B. B.; Warmus, J. S.; Moriarty, K. J. J. Org. Chem. 1991, 56, 1192.

    32. [32]

      (a) Wang, L. C.; Luis, A. L.; Agaplou, K.; Jang, H. Y.; Krische, M. J. J. Am. Chem. Soc. 2002, 124, 2402.
      (b) Frank, S. A.; Mergott, D. J.; Roush, W. R. J. Am. Chem. Soc. 2002, 124, 2404.

    33. [33]

      Bai, Y.; Shen, X. Y.; Li, Y.; Dai, M. J. J. Am. Chem. Soc. 2016, 138, 10838.  doi: 10.1021/jacs.6b07585

    34. [34]

      (a) Wilson, R. M.; Jen, W. S.; MacMillan, D. W. C. J. Am. Chem. Soc. 2005, 127, 11616.
      (b) Lambert, T. H.; Danishefsky, S. J. J. Am. Chem. Soc. 2006, 128, 426.

    35. [35]

      (a) Davis, D. C.; Walker, K. L.; Hu, C.; Zare, R. N.; Waymouth, R. M.; Dai, M. J. J. Am. Chem. Soc. 2016, 138, 10693.
      (b) Bai, Y.; Davis, D. C.; Dai, M. J. Angew. Chem., Int. Ed. 2014, 53, 6519.
      (c) Gehrtz, P. H.; Hirschbeck, V.; Ciszek, B.; Fleischer, I. Synthesis 2016, 48, 1573.
      (d) Wu, X. F.; Neumann, H.; Beller, M. Chem. Rev. 2013, 113, 1.
      (e) Wu, X.-F.; Neumann, H.; Beller, M. Chem. Rev. 2013, 113, 1.
      (f) Bai, Y.; Davis, D. C.; Dai, M. J. J. Org. Chem. 2017, 82, 2319.

    36. [36]

      (a) Li, Y.; Yang, Y.; Yu, B. Tetrahedron Lett. 2008, 49, 3604.
      (b) Yang, Y.; Li, Y.; Yu, B. J. Am. Chem. Soc. 2009, 131, 12076.
      (c) Yu, B.; Sun, J.; Yang, X. Acc. Chem. Res. 2012, 45, 1227.
      (d) Nie, S.; Li, W.; Yu, B. J. Am. Chem. Soc. 2014, 136, 4157.

    37. [37]

      Kim, H. J.; Choi, S.-H.; Jeon, B.-S.; Kim, N.; Pongdee, R.; Wu, Q.; Liu, H.-W. Angew. Chem., Int. Ed. 2014, 53, 13553.  doi: 10.1002/anie.201407806

    38. [38]

      Kim, H. J.; Pongdee, R.; Wu, Q.; Hong, L.; Liu, H.-W. J. Am. Chem. Soc. 2007, 129, 14582.  doi: 10.1021/ja076580i

    39. [39]

      (a) Kim, H. J.; Ruszczycky, M. W.; Choi, S.-H.; Liu, Y.-N.; Liu, H.-W. Nature 2011, 473, 109.
      (b) Kim, H. J.; Ruszczycky, M. W.; Liu, H.-W. Curr. Opin. Chem. Biol. 2012, 16, 124.
      (a) Oikawa, H. Bull. Chem. Soc. Jpn. 2005, 78, 537.

    40. [40]

      (a) Chen, Y.-L.; Chen, Y.-H.; Lin, Y.-C.; Tsai, K.-C.; Chiu, H.-T. J. Biol. Chem. 2009, 284, 7352.
      (b) Kim, H. J.; White-Phillip, J. A.; Ogasawara, Y.; Shin, N.; Isiorho, E. A.; Liu, H.-W. J. Am. Chem. Soc. 2010, 132, 2901.
      (c) Isiorho, E. A.; Liu, H.-w.; Keatinge-Clay, A. T. Biochemistry 2012, 51, 1213.

    41. [41]

      Yang, Y. L.; Lu, C. P.; Chen, M. Y.; Chen, K. Y.; Wu, Y. C.; Wu, S. H. Chem.-Eur. J. 2007, 13, 6985.  doi: 10.1002/(ISSN)1521-3765

    42. [42]

      Shionozaki, N.; Yamaguchi, T.; Kitano, H.; Tomizawa, M.; Makino, K.; Uchiro, H. Tetrahedron Lett. 2012, 53, 5167.  doi: 10.1016/j.tetlet.2012.07.058

    43. [43]

      Nicolaou, K.; Shi, L.; Lu, M.; Pattanayak, M. R.; Shah, A. A.; Ioannidou, H. A.; Lamani, M. Angew. Chem., Int. Ed. 2014, 53, 10970.  doi: 10.1002/anie.201406815

    44. [44]

      Li, L.; Yu, P.; Tang, M.-C.; Zou, Y.; Gao, S-S.; Hung, Y.-S.; Zhao, M.; Watanabe, K.; Houk, K. N.; Tang, Y. J. Am. Chem. Soc. 2016, 138, 15837.  doi: 10.1021/jacs.6b10452

    45. [45]

      Burmeister, H. R.; Bennet, G. A.; Vesonder, R. F.; Hesseltine, C. W. Antimicrob. Agents Chemother. 1974, 5, 634.  doi: 10.1128/AAC.5.6.634

    46. [46]

      Turos, E.; Audia, J. E.; Danishefsky, S. J. J. Am. Chem. Soc. 1989, 111, 8231.  doi: 10.1021/ja00203a026

    47. [47]

      (a) Burke, L. T.; Dixon, D. J.; Ley, S. V.; Rodríguez, F. Org. Lett. 2000, 2, 3611.
      (b) Burke, L. T.; Dixon, D. J.; Ley, S. V.; Rodríguez, F. Org. Biomol. Chem. 2005, 3, 274.

    48. [48]

      Kumiko, Y. K.; Shindo, M.; Shishido, K. Tetrahedron Lett. 2001, 42, 2517.  doi: 10.1016/S0040-4039(01)00217-9

    49. [49]

      Yin, J.; Wang, C.; Kong, L.; Cai, S.; Gao, S. Angew. Chem., Int. Ed. 2012, 51, 7786.  doi: 10.1002/anie.201202455

    50. [50]

    51. [51]

      (a) Oikawa, H. Cell Chem. Biol. 2016, 23, 429.
      (b) Oikawa, H.; Tokiwano, T. Nat. Prod. Rep. 2004, 21, 321.
      (c) Klas, K.; Tsukamoto, S.; Sherman, D. H.; Williams, R. M. J. Org. Chem. 2015, 80, 11672.
      (d) Minami, A.; Oikawa, H. J. Antibiot. 2016, 1.
      (e) Oikawa, H. Bull. Chem. Soc. 2005, 78, 537.
      (f) Jeon, B.-S.; Wang, S.-A.; Ruszczycky, M. W.; Liu, H.-W. Chem. Rev. 2017, 117, 5367.

    52. [52]

      (a) Wu, Q.; Wu, Z.; Qu, X.; Liu, W. J. Am. Chem. Soc. 2012, 134, 17342.
      (b) Tian, Z.; Sun, P.; Yan, Y.; Wu, Z.; Zheng, Q.; Zhou, X.; Zhang, H.; Yu, F.; Jia, X.; Chen, D.; Mandi, A.; Kurtan T.; Liu, W. Nat. Chem. Biol. 2015, 11, 259.
      (c) Pang, B.; Zhong, G.; Tang, Z.; Liu, W. Methods Enzymol. 2016, 575, 39.
      (d) Zheng, Q.; Tian, Z.; Liu, W. Curr. Opin. Chem. Biol. 2016, 31, 95.
      (e) Zheng, Q.; Guo, Y.; Yang, L.; Zhao, Z.; Wu, Z.; Zhang, H.; Liu, J.; Cheng, X.; Wu, J.; Yang, H.; Jiang, H.; Pan, L.; Liu, W. Cell Chem. Biol. 2016, 23, 352.
      (f) Zheng, Q.; Gong, Y.; Guo, Y.; Zhao, Z.; Wu, Z.; Zhou, Z.; Chen, D.; Pan, L.; Liu, W. Cell Chem. Biol. 2018, 25, 718.

    53. [53]

      Kato, N.; Nogawa, T.; Hirota, H.; Jang, J. H.; Takahashi, S.; Ahn, J. S.; Osada, H. Biochem. Biophys. Res. Commun. 2015, 460, 210.  doi: 10.1016/j.bbrc.2015.03.011

    54. [54]

      Li, X.; Zheng, Q.; Yin, J.; Liu, W.; Gao, S. Chem. Commun. 2017, 53, 4695.  doi: 10.1039/C7CC01929G

  • 加载中
    1. [1]

      Yuheng Zhou . 大学课堂的色彩——探索过渡元素的美. University Chemistry, 2025, 40(6): 303-309. doi: 10.12461/PKU.DXHX202407110

    2. [2]

      Ben Yang ,  Shukun Shen ,  Pujun Jin ,  Yujia Luo ,  Jianyong Hu . Covalent organic frameworks: emerging organic porous materials. University Chemistry, 2026, 41(4): 264-274. doi: 10.12461/PKU.DXHX202502128

    3. [3]

      Liangzhen Hu ,  Li Ni ,  Ziyi Liu ,  Xiaohui Zhang ,  Bo Qin ,  Yan Xiong . A Green Chemistry Experiment on Electrochemical Synthesis of Benzophenone. University Chemistry, 2024, 39(6): 350-356. doi: 10.3866/PKU.DXHX202312001

    4. [4]

      Renxiu Zhang ,  Xin Zhao ,  Yunfei Zhang . Application of Electrochemical Synthesis in the Teaching of Organic Chemistry. University Chemistry, 2025, 40(4): 174-180. doi: 10.12461/PKU.DXHX202406116

    5. [5]

      Li Jiang ,  Changzheng Chen ,  Yang Su ,  Hao Song ,  Yanmao Dong ,  Yan Yuan ,  Li Li . Electrochemical Synthesis of Polyaniline and Its Anticorrosive Application: Improvement and Innovative Design of the “Chemical Synthesis of Polyaniline” Experiment. University Chemistry, 2024, 39(3): 336-344. doi: 10.3866/PKU.DXHX202309002

    6. [6]

      Fei Liu ,  Dong-Yang Zhao ,  Kai Sun ,  Ting-Ting Yu ,  Xin Wang . Comprehensive Experimental Design for Photochemical Synthesis, Analysis, and Characterization of Seleno-Containing Medium-Sized N-Heterocycles. University Chemistry, 2024, 39(3): 369-375. doi: 10.3866/PKU.DXHX202309047

    7. [7]

      Tingting Yu ,  Si Chen ,  Lianglong Sun ,  Tongtong Shi ,  Kai Sun ,  Xin Wang . Comprehensive Experimental Design for the Photochemical Synthesis, Analysis, and Characterization of Difluoropyrroles. University Chemistry, 2024, 39(11): 196-203. doi: 10.3866/PKU.DXHX202401022

    8. [8]

      Lutian Zhao , Yangge Guo , Liuxuan Luo , Xiaohui Yan , Shuiyun Shen , Junliang Zhang . Electrochemical Synthesis for Metallic Nanocrystal Electrocatalysts: Principle, Application and Challenge. Acta Physico-Chimica Sinica, 2024, 40(7): 2306029-0. doi: 10.3866/PKU.WHXB202306029

    9. [9]

      Mengyun Wu ,  Yuxin Deng ,  Wenhui Wang ,  Dongdong Xu ,  Langui Xie ,  Peipei Sun . 电化学合成4-氯-2-三异丙基硅基喹啉. University Chemistry, 2026, 41(5): 222-229. doi: 10.12461/PKU.DXHX202511044

    10. [10]

      Caixia Lin ,  Zhaojiang Shi ,  Yi Yu ,  Jianfeng Yan ,  Keyin Ye ,  Yaofeng Yuan . Ideological and Political Design for the Electrochemical Synthesis of Benzoxathiazine Dioxide Experiment. University Chemistry, 2024, 39(2): 61-66. doi: 10.3866/PKU.DXHX202309005

    11. [11]

      Jia-He Li ,  Yu-Ze Liu ,  Jia-Hui Ma ,  Qing-Xiao Tong ,  Jian-Ji Zhong ,  Jing-Xin Jian . 洛芬碱衍生物的合成、化学发光与重金属离子检测. University Chemistry, 2025, 40(6): 230-237. doi: 10.12461/PKU.DXHX202407080

    12. [12]

      Lixing ZHANG , Yaowen WANG , Xu HAN , Junhong ZHOU , Jinghui WANG , Liping LI , Guangshe LI . Research progress in the synthesis of fluorine-containing perovskites and their derivatives. Chinese Journal of Inorganic Chemistry, 2025, 41(9): 1689-1701. doi: 10.11862/CJIC.20250007

    13. [13]

      Weizhe Liu ,  Minghui Shi ,  Ruiqi Zhu ,  Bin Pan ,  Guofu Huang . 抗癌药物艾乐替尼的生物电子等排体的合成. University Chemistry, 2026, 41(5): 210-221. doi: 10.12461/PKU.DXHX202510066

    14. [14]

      Chengyan XU , Jiangnan YU , Yu LI , Xizhen PAN , Yinlin HOU , Wenmin WANG . Synthesis, structure, and bioactivity of a Ho4 complex bridged by azide group. Chinese Journal of Inorganic Chemistry, 2026, 42(7): 1453-1462. doi: 10.11862/CJIC.20260033

    15. [15]

      Pingping Liu ,  Dandan Tang ,  Zhifeng Li ,  Xiaowen Han ,  Guoling Zhang ,  Pu Chen ,  Hai-Tao Feng . 古今“色”界碰撞——天然染料与合成染料的布艺实验. University Chemistry, 2026, 41(8): 250-259. doi: 10.12461/PKU.DXHX202507099

    16. [16]

      Yurong Tang ,  Yunren Shi ,  Yi Xu ,  Bo Qin ,  Yanqin Xu ,  Yunfei Cai . Innovative Experiment and Course Transformation Practice of Visible-Light-Mediated Photocatalytic Synthesis of Isoquinolinone. University Chemistry, 2024, 39(5): 296-306. doi: 10.3866/PKU.DXHX202311087

    17. [17]

      Bin SUN , Heyan JIANG . Glucose-modified bis-Schiff bases: Synthesis and bio-activities in Alzheimer′s disease therapy. Chinese Journal of Inorganic Chemistry, 2025, 41(7): 1338-1350. doi: 10.11862/CJIC.20240428

    18. [18]

      Longfei MA , Fang SI , Congjie PAN , Xinhua WANG . Synthesis and crystal structure of extended tetrathiafulvalene derivatives and cupric bromide charge transfer complexes. Chinese Journal of Inorganic Chemistry, 2026, 42(6): 1229-1236. doi: 10.11862/CJIC.20250355

    19. [19]

      Mengyang LI , Zhonghao NIU , Hao XU , Jingli XIE . One-pot synthesis of 4H-pyran derivatives catalyzed by viologen-modified metal-organic frameworks. Chinese Journal of Inorganic Chemistry, 2026, 42(7): 1513-1522. doi: 10.11862/CJIC.20250205

    20. [20]

      Chunyan Hu ,  Wei Wang ,  Zewei Mao ,  Mei Zhang ,  Lei Zhang ,  Yuping Lin . Three-stage progressive teaching reform and practice in organic chemistry experiments for pharmacy undergraduates: synthesis of coumarin-chalcone derivatives. University Chemistry, 2026, 41(7): 282-289. doi: 10.12461/PKU.DXHX202505011

Metrics
  • PDF Downloads(184)
  • Abstract views(7836)
  • HTML views(2242)

通讯作者: 陈斌, bchen63@163.com
  • 1. 

    沈阳化工大学材料科学与工程学院 沈阳 110142

  1. 本站搜索
  2. 百度学术搜索
  3. 万方数据库搜索
  4. CNKI搜索
Address:Zhongguancun North First Street 2,100190 Beijing, PR China Tel: +86-010-82449177-888
Powered By info@rhhz.net

/

DownLoad:  Full-Size Img  PowerPoint
Return