Citation: Zhang Qiying, Zhang Yiming, Hao Erjun, Bai Juan, Qu Guirong, Guo Haiming. Asymmetric Transfer Hydrogenation via Dynamic Kinetic Resolution for the Construction of Carbocyclic N3-Purine Nucleosides[J]. Chinese Journal of Organic Chemistry, ;2020, 40(2): 376-383. doi: 10.6023/cjoc201907053 shu

Asymmetric Transfer Hydrogenation via Dynamic Kinetic Resolution for the Construction of Carbocyclic N3-Purine Nucleosides

  • Corresponding author: Guo Haiming, ghm@htu.edu.cn
  • Received Date: 30 July 2019
    Revised Date: 30 September 2019
    Available Online: 25 February 2019

    Fund Project: the National Natural Science Foundation of China U1604283the Overseas Expertise Introduction Project for Discipline Innovation D17007the National Natural Science Foundation of China 21602045Project supported by the National Natural Science Foundation of China (Nos. 21602045, U1604283), and the Overseas Expertise Introduction Project for Discipline Innovation (111 Project, No. D17007)

Figures(4)

  • N3-Purine nucleoside can be employed as a potent dual inhibitor to inhibit viruses more effectively because it could be possibly recognized by both purine-and pyrimidine-metabolizing enzymes. Herein, an asymmetric transfer hydrogenation via dynamic kinetic resolution of rac-α-(purin-3-yl)cyclopentones has been developed to produce a wide range of carbocyclic N3-purine nucleosides in high yields and excellent stereoselectivities. Moreover, the catalytic system was suitable for rac-α-pyrimidinyl cyclopentones. With additional transformations, several 2'-F-, AcS-, N3-modified carbocyclic nucleosides could be obtained with good to excellent yields and excellent enantioselectivities.
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    1. [1]

      (a) Zhou, H.; Zeng, X.; Ding, L.; Xie, Y.; Zhong, G. Org. Lett. 2015, 17, 2385.
      (b) Trost, B. M.; Madsen, R.; Guile, S. D.; Brown, B. J. Am. Chem. Soc. 2000, 122, 5947.
      (c) Kakuda, T. N. Clin. Ther. 2000, 22, 685.
      (d) Boutureira, O.; Matheu, M. I.; Díaz, Y.; Castillón, S. Chem. Soc. Rev. 2013, 42, 5056.
      (e) Forsman, J. J.; Leino, R. Chem. Rev. 2011, 111, 3334.
      (f) Lebreton, J.; Escudier, J.-M.; Arzel, Len, C. Chem. Rev. 2010, 110, 3371.
      (g) Amblard, F.; Cho, J. H.; Schinazi, R. F. Chem. Rev. 2009, 109, 4207.
      (h) Liu, Y.; Guo, X.; Bai, P. Chin. J. Org. Chem. 2014, 34, 2202 (in Chinese).
      (刘亚君, 郭翔海, 白鹏, 有机化学, 2014, 34, 2202.)
      (i) Fan, X.-S; Zhang, X.-Y.; Wang, X.; Qu, G.-R. Chin. J. Org. Chem. 2008, 28, 1888 (in Chinese).
      (范学森, 张新迎, 王霞, 渠桂荣, 有机化学, 2008, 28, 1888.)

    2. [2]

      (a) Barral, K.; Courcambeck, J.; Pèpe, G.; Balzarini, J.; Neyts, J.; Clercq, E. D.; Camplo, M. J. Med. Chem. 2005, 48, 450.
      (b) Keane, S. J.; Ford, A.; Mullins, N. D.; Maguire, N. M.; Legigan, T.; Balzarini, J.; Maguire, A. R. J. Org. Chem. 2015, 80, 2479.
      (c) Gai, X.; Song, W.; Heng, S.; Yang, W. Chin. J. Integr. Tradit. West. Med. Liver Dis. 2005, 15, 50 (in Chinese).
      (盖欣, 宋万玲, 桓树学, 杨文东, 中西医结合肝病杂志, 2005, 15, 50.)

    3. [3]

      (a) Hu, L.; Ren, Y.; Ramström, O. J. Org. Chem. 2015, 80, 8478.
      (b) Singh, U. S.; Mishra, R. C.; Shankar, R.; Chu, C. K. J. Org. Chem. 2014, 79, 3917.
      (c) Caso, M. F.; D'Alonzo, D.; D'Errico, S.; Palumbo, G.; Guaragna, A. Org. Lett. 2015 17, 2626.

    4. [4]

      (a) Silverman, R. B. The Organic Chemistry of Drug Design and Drug Action, Elsevier, Evanston, 2004.
      (b) Kompis, I. M.; Islam, K.; Then, R. L. Chem. Rev. 2005, 105, 583.
      (c) Lyon, M. A.; Ducruet, A. P.; Wipf, P.; Lazo, J. S. Nat. Rev. Drug Disc. 2002, 1, 961.
      (d) Gangjee, A.; Li, W.; Yang, J.; Kisliuk, R. L. J. Med. Chem. 2008, 51, 68.

    5. [5]

      (a) Jeong, L. S.; Lee, J. A. Antiviral Chem. Chemother. 2004, 15, 235.
      (b) Liu, Y.; Guo, X.; Bai, P. Chin. J. Org. Chem. 2014, 34, 2202.
      (c) Boutureira, O.; Matheu, M. I.; Díaz, Y.; Castillón, S. Chem. Soc. Rev. 2013, 42, 5056.

    6. [6]

      (a) Xie, M.-S.; Wang, Y.; Li, J.-P.; Du, C.; Zhang, Y.-Y.; Hao, E.-J.; Zhang, Y.-M.; Qu, G.-R.; Guo, H.-M. Chem. Commun. 2015, 51, 12451.
      (b) Huang, K.-X.; Xie, M.-S.; Zhang, Q.-Y.; Niu, H.-Y.; Qu, G.-R.; Guo, H.-M. Org. Lett. 2018, 20, 5398.
      (c) Wang, J.; Zhang, Q.-Y.; Xie, M.-S.; Wang, D.-C.; Qu, G.-R.; Guo, H.-M. Org. Lett. 2018, 20, 6578.
      (d) Gao, Y.-W.; Niu, H.; Zhang, Q.-Y.; Xie, M.; Qu, G.; Guo, H. Adv. Synth. Catal. 2018, 360, 2813.

    7. [7]

      (a) Bhat, B.; Neelima, N. J.; Leonard, H.; Robinson, A.; Wang, H.-J. J. Am. Chem. Soc. 1996, 118, 3065.
      (b) Leonard, N. J.; Laursenf, R. A. Biosci., Biotechnol., Biochem. 1965, 4, 354.

    8. [8]

      (a) Sadler, J. M.; Mosley, S. L.; Dorgan, K. M.; Zhou, Z. S.; Seley-Radtke, K. L. Bioorg. Med. Chem. 2009, 17, 5520.
      (b) Jiang, M. X.-W.; Warshakoon, N. C.; Miller, M. J. J. Org. Chem. 2005, 70, 2824.

    9. [9]

      (a) Tang, W.; Zhang, X. Chem. Rev. 2003, 103, 3029.
      (b) Liu, S.; Xie, J.-H.; Wang, L.-X.; Zhou, Q.-L. Angew. Chem. 2007, 119, 7650; Angew. Chem., Int. Ed. 2007, 46, 7506.
      (c) Liu, S.; Xie, J.-H.; Li, W.; Kong, W.-L.; Wang, L.-X.; Zhou, Q.-L. Org. Lett. 2009, 11, 4994.
      (d) Zhou, Q.; Xie, J.; Zhu, S.; Wang, L. Tianjin Sci. Technol. 2014, 41, 11 (in Chinese).
      (周其林, 谢建华, 朱守非, 王立新, 天津科技, 2014, 41, 11.)

    10. [10]

      (a) Zhang, Q.; Ma, B.-W.; Wang, Q.-.Q.; Wang, X.-X.; Hu, X.; Xie, M.-S.; Qu, G.-R.; Guo, H.-M. Org. Lett. 2014, 16, 2014.
      (b) Vyas, V. K.; Bhanage, B. M. Org. Lett. 2016, 18, 6436.
      (c) Matsunami, A.; Ikeda, M.; Nakamura, H.; Yoshida, M.; Kuwata, S.; Kayaki, Y. Org. Lett. 2018, 20, 5213.
      (d) Vyas, V. K.; Bhanage, B. M. Asian J. Org. Chem. 2018, 7, 346.
      (e) Liu, Q.; Wang, C.; Zhou, H.; Wang, O.; Lv, J.; Cao, Lu; Fu, Y. Org. Lett. 2018, 20, 971.

    11. [11]

      (a) Zhang, Y.-M.; Zhang, Q.-Y.; Wang, D.-C.; Xie, M.-S.; Qu, G.-R.; Guo, H.-M. Org. Lett. 2019, 21, 2998.
      (b) Sun, H.-L.; Chen, F.; Xie, M.-S.; Guo, H.-M.; Qu, G.-R.; He, Y.-M.; Fan, Q.-H. Org. Lett. 2016, 18, 2260.

    12. [12]

      (a) Chan, A. S. C.; Pluth, J. J.; Halpern, J. J. Am. Chem. Soc. 1980, 102, 5952.
      (b) Miyashita, A.; Yasuda, A.; Takaya, H.; Toriumi, K.; Ito, T.; Souchi, T.; Noyori, R. J. Am. Chem. Soc. 1980, 102, 7932.

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