Citation: Yang Quanli, Song Yuye, Yu Ping, Wang Long, Liu Mingguo, Huang Nianyu. 1, 8-Diazabicyclo[5.4.0]undec-7-ene (DBU)-Promoted Stere-oselective Synthesis of Oxazolidin-2-(thi)one Derivatives[J]. Chinese Journal of Organic Chemistry, ;2017, 37(12): 3177-3185. doi: 10.6023/cjoc201704036 shu

1, 8-Diazabicyclo[5.4.0]undec-7-ene (DBU)-Promoted Stere-oselective Synthesis of Oxazolidin-2-(thi)one Derivatives

  • Corresponding author: Huang Nianyu, hny115@126.com
  • Received Date: 21 April 2017
    Revised Date: 10 August 2017
    Available Online: 8 December 2017

    Fund Project: the National Natural Science Foundation of China 21602123Project supported by the National Natural Science Foundation of China (No. 21602123), the Youth Talent Development Foundation and Scientific Foundation from Graduate School of China Three Gorges University (No. SDYC2016121)the Youth Talent Development Foundation and Scientific Foundation from Graduate School of China Three Gorges University SDYC2016121

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  • A series of multi-substituted oxazolidin-2-(thi)one derivatives were prepared via 1, 8-diazabicyclo[5.4.0]undec-7-ene (DBU) promoted nucleophilic addition/cyclization from alkynyl alcohol and isocynate or thiocynate in high yields of 75%~95%. This concise and efficient approach provides a facial access to a library of biological (Z)-arylmethylene substituted oxazolidin-2-(thi)one derivatives with high stereo-selectivities.
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    1. [1]

      Zappia, G.; Menendez, P.; Monache, G. D.; Misiti, D.; Nevola, L.; Botta, B. Mini-Rev. Med. Chem. 2007, 7, 389.  doi: 10.2174/138955707780363783

    2. [2]

      (a) Phillips, O. A.; Sharaf, L. H. Expert Opin. Ther. Pat. 2016, 26, 591.
      (b) Jadhavar, P. S.; Vaja, M. D.; Dhameliya, T. M.; Chakraborti, A. K. Curr. Med. Chem. 2015, 22, 4379.

    3. [3]

      (a) Fujita, T.; Yamago, S. Chem.-Eur. J. 2015, 21, 18547.
      (b) Green, R.; Peed, J.; Taylor, J. E.; Blackburn, R. A.; Bull, S. D. Nat. Protoc. 2013, 8, 1890.

    4. [4]

      Ferreira, J.; Rees-Jones, S. C.; Ramaotsoa, V.; Msutu, A.; Hunter, R. Org. Biomol. Chem. 2016, 14, 1545.  doi: 10.1039/C5OB02560E

    5. [5]

      (a) Guo, B.; Fan, H.; Xin, Q.; Chu, W.; Wang, H.; Huang, Y.; Chen, X.; Yang, Y. J. Med. Chem. 2013, 56, 2642.
      (b) Friggeri, L.; Ballante, F.; Ragno, R.; Musmuca, I.; De Vita, D.; Manetti, F.; Biava, M.; Scipione, L.; Di Santo, R.; Costi, R.; Feroci, M.; Tortorella, S. J. Chem. Inf. Model. 2013, 53, 1463.

    6. [6]

      (a) Njiojob, C. N.; Bozell, J. J.; Long, B. K.; Elder, T.; Key, R. E.; Hartwig, W. T. Chem.-Eur. J. 2016, 22, 12506.
      (b) Mydock-McGrane, L.; Rath, N. P.; Covey, D. F. J. Org. Chem. 2014, 79, 5636.

    7. [7]

      Mendes, R. E.; Deshpande, L. M.; Jones, R. N. Drug Resist. Updates 2014, 17, 1.  doi: 10.1016/j.drup.2014.04.002

    8. [8]

      Chahine, E. B.; Sucher, A. J.; Knutsen, S. D. Consult. Pharm. 2015, 30, 386.  doi: 10.4140/TCP.n.2015.386

    9. [9]

      (a) Xu, J. X.; Zhao, J. W.; Jia, Z. B. Chin. Chem. Lett. 2011, 22, 1063.
      (b) Li, Y. W.; Liu, Y.; Jia, Y. C.; Yuan, J. Y. Chin. Chem. Lett. 2013, 24, 230.

    10. [10]

      (a) Sadeghzadeh, S. M. Appl. Organomet. Chem. 2016, 30, 835.
      (b) Bacchi, A.; Chiusoli, G. P.; Costa, M.; Gabriele, B.; Righi, C.; Salerno, G. Chem. Commun. 1997, 1209.
      (c) Song, Q. W.; Zhou, Z. H.; Wang, M. Y.; Zhang, K.; Liu, P.; Xun, J. Y.; He, L. N. ChemSusChem 2016, 9, 2054.
      (d) Hu, J.; Ma, J.; Zhu, Q.; Zhang, Z.; Wu, C.; Han, B. Angew. Chem., Int. Ed. 2015, 54, 5399.
      (e) Hase, S.; Kayaki, Y.; Ikariya, T. ACS Catal. 2015, 5, 5135.

    11. [11]

      (a) Fujisaki, F.; Abe, N.; Sumoto, K. Heterocycles 2008, 75, 1681.
      (b) Steiner, B.; Langer, V.; Koóš, M. Carbohydr. Res. 2009, 344, 2079.

    12. [12]

      a) Li, S. Q.; Xiong, P.; Zhu, L.; Qian, X. Y.; Xu, H. C. Eur. J. Org. Chem. 2016, 2016, 3449.
      (b) Sekine, K.; Mawatari, T.; Yamada, T. Synlett 2015, 26, 2447.
      (c) Kim, W. S.; Yoon, E.; Jo, K. A.; Kang, E. J. Bull. Korean Chem. Soc. 2011, 32, 3158.

    13. [13]

      (a) Lu, X. F.; Yang, Z.; Huang, N. Y.; He, H. B.; Deng, W. Q.; Zou, K. Bioorg. Med. Chem. Lett. 2015, 25, 3726.
      (b) Wang, L.; Xie, Y. B.; Huang, N. Y.; Yan, J. Y.; Hu, W. M.; Liu, M. G.; Ding, M. W. ACS Catal. 2016, 6, 4010.
      (c) Li, R. K.; Yang, Q. L.; Liu, Y.; Li, D. W.; Huang, N. Y.; Liu, M. G. Chin. Chem. Lett. 2016, 27, 345.

    14. [14]

      Li, S.; Ye, J.; Yuan, W.; Ma, S. Tetrahedron 2013, 69, 10450.  doi: 10.1016/j.tet.2013.09.087

    15. [15]

      Zhao, J.; Huang, H.; Qi, C.; Jiang, H. Eur. J. Org. Chem. 2012, 29, 5665.

    16. [16]

      (a) Ritter, S.; Horino, Y.; Lex, J.; Schmalz, H. G. Synlett 2006, 3309.
      (b) Ramesh, R.; Chandrasekaran, Y.; Megha, R.; Chandrasekaran, S. Tetrahedron 2007, 63, 9153.
      (c) Hu, M.; Song, R. J.; Li, J. H. Angew. Chem., Int. Ed. 2015, 54, 608.

    17. [17]

      (a) Doherty, S.; Knight, J. G.; Perry, D. O.; Ward, N. A.; Bittner, D. M.; McFarlane, W.; Probert, M. R. Organometallics 2016, 35, 1265.
      (b) Wang, F.; Wang, Y.; Cai, L.; Miao, Z.; Chen, R. Adv. Synth. Catal. 2008, 350, 2733.
      (c) Hu, Y.; Xin, X.; Wan, B. Tetrahedron Lett. 2014, 55, 32.

    18. [18]

      (a) Hashmi, A.; Stephen K.; Wang, T.; Shi, S.; Rudolph, M. J. Org. Chem. 2012, 77, 7761.
      (b) Engel, D. A.; Dudley, G. B. Org. Lett. 2006, 8, 4027.
      (c) Jagtap, S. R.; Bhanage, B. M. J. Chem. Res. 2007, 6, 370.
      (d) Smissman, E. E.; Johnsen, R. H.; Carlson, A. W.; Aycock, B. F. J. Org. Chem. 1956, 78, 3395.
      (e) Cooper, M. A.; Lucas, M. A.; Taylor, J. M.; Ward, A. D.; Williamson, N. M. Synthesis 2001, 621.
      (f) Moran, W. J.; Rodríguez, A. Org. Biomol. Chem. 2012, 10, 8590.
      (g) Zhang, H.; Tanimoto, H.; Morimoto, T.; Nishiyama, Y.; Kakiuchi, K. Org. Lett. 2013, 20, 5222.

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