Citation: Zhang Xiong, Feng Kaixiang, Xia Aibao. Asymmetric Organocatalytic Construction of Functionalized Bicyclic Lactams[J]. Chinese Journal of Organic Chemistry, ;2018, 38(12): 3373-3380. doi: 10.6023/cjoc201806010 shu

Asymmetric Organocatalytic Construction of Functionalized Bicyclic Lactams

  • Corresponding author: Zhang Xiong, xiongzhang1212@126.com Xia Aibao, xiaaibao@zjut.edu.cn
  • Received Date: 7 June 2018
    Revised Date: 20 August 2018
    Available Online: 5 December 2018

    Fund Project: Project supported by the Natural Science Foundation of Zhejiang Province (No. LY18B020017)the Natural Science Foundation of Zhejiang Province LY18B020017

Figures(2)

  • A novel enantioselective organocatalytic cascade Michael-hemiaminalization-hemiacetalization reaction of α, β-unsaturated aldehydes with α-ketoamides as binucleophiles has been developed. A series of chiral functionalized bicyclic lactams with two cis contiguous stereogenic centers have been synthesized in up to 97% yield with up to >20:1 dr and up to >99% ee.
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    1. [1]

      For selected recent reviews of the asymmetric domino reactions, see: (a) Grondal, C.; Jeanty, M.; Enders, D. Nat. Chem. 2010, 2, 167.
      (b) Albrecht, Ł.; Jiang, H.; Jørgensen, K. A. Angew. Chem., Int. Ed. 2011, 50, 8492.
      (c) Pellissier, H. Adv. Synth. Catal. 2012, 354, 237.
      (d) Volla, C. M. R.; Atodiresei, I.; Rueping, M. Chem. Rev. 2014, 114, 2390.
      (e) Wang, Y.; Lu, H.; Xu, P.-F. Acc. Chem. Res. 2015, 48, 1832.
      (f) Donslund, B. S.; Johansen, T. K.; Poulsen, P. H.; Halskov, K. S.; Jørgensen, K. A. Angew. Chem., Int. Ed. 2015, 54, 13860.

    2. [2]

      (a) Dickmeiss, G.; Jensen, K. L.; Worgull, D.; Franke, P. T.; Jørgensen, K. A. Angew. Chem., Int. Ed. 2011, 50, 1580.
      (b) Zhang, X.-S.; Song, X.-X.; Li, H.; Zhang, S.-L.; Chen, X.-B.; Yu, X.-H.; Wang, W. Angew. Chem., Int. Ed. 2012, 51, 7282.
      (c) Zhang, J.-X.; Li, N. K.; Liu, Z.-M.; Huang, X. F.; Geng, Z.-C.; Wang, X.-W. Adv. Synth. Catal. 2013, 355, 797.
      (d) Han, B.; Huang, W.; Ren, W.; He, G.; Wang, J.-H.; Peng, C. Adv. Synth. Catal. 2015, 357, 561

    3. [3]

      Bonne, D.; Constantieux, T.; Coquerel, Y.; Rodriguez, J. Chem.-Eur. J. 2013, 19, 2218.  doi: 10.1002/chem.v19.7

    4. [4]

      (a) Trost, B. M.; Schroeder, G. M. J. Am. Chem. Soc. 2000, 122, 3785.
      (b) Trost, B. M.; Dong, G. B.; Vance, J. A. Chem.-Eur. J. 2010, 16, 6265.
      (c) Raimondi, W.; Bonne, D.; Rodriguez, J. Angew. Chem., Int. Ed. 2012, 51, 40.
      (d) Raimondi, W.; Bonne, D.; Rodriguez, J. Chem. Commun. 2012, 48, 6763.

    5. [5]

      Dambruoso, P.; Massi, A.; Dondoni, A. Org. Lett. 2005, 7, 4657.  doi: 10.1021/ol051809p

    6. [6]

      Vincent, J.-M.; Margottin, C.; Berlande, M.; Cavagnat, D.; Buffeteau, T.; Landais, Y. Chem. Commun. 2007, 43, 4782.
       

    7. [7]

      Zhang, B.-Y.; Jiang, Z.-X.; Zhou, X.; Lu, S.-M.; Li, J.; Liu, Y.; Li, C. Angew. Chem., Int. Ed. 2012, 51, 13159.  doi: 10.1002/anie.201206438

    8. [8]

      (a) Rueping, M.; Kuenkel, A.; Tato, F.; Bats, J. W. Angew. Chem., Int. Ed. 2009, 48, 3699.
      (b) Rueping, M.; Kuenkel, A.; Frçlich, R. Chem.-Eur. J. 2010, 16, 4173.

    9. [9]

      (a) Ding, D.; Zhao, C.-G.; Guo, Q.; Arman, H. Tetrahedron 2010, 66, 4423.
      (b) Ding, D.; Zhao, C.-G. Tetrahedron Lett. 2010, 51, 1322.

    10. [10]

      Lefranc, A.; Guénée, L.; Alexakis, A. Org. Lett. 2013, 15, 2172.  doi: 10.1021/ol400697n

    11. [11]

      (a) Baslé, O.; Raimondi, W.; Sanchez Duque, M. M.; Bonne, D.; Constantieux, T.; Rodriguez, J. Org. Lett. 2010, 12, 5246.
      (b) Shi, D.; Xie, Y.; Zhou, H.; Xia, C.; Huang, H. Angew. Chem., Int. Ed. 2012, 51, 1248.
      (c) Goudedranche, S.; Pierrot, D.; Constantieux, T.; Bonne, D.; Rodriguez, J. Chem. Commun. 2014, 50, 15605.

    12. [12]

      (a) Xu, D.-Q.; Xia, A.-B.; Luo, S.-P.; Tang, J.; Zhang, S.; Jiang, J.-R.; Xu, Z.-Y. Angew. Chem., Int. Ed. 2009, 48, 3821.
      (b) Xia, A.-B.; Xu, D.-Q.; Luo, S.-P.; Jiang, J.-R.; Tang, J.; Wang, Y.-F.; Xu, Z.-Y. Chem.-Eur. J. 2010, 16, 801.
      (c) Xia, A.-B.; Wu, C.; Wang, T.; Zhang, Y.-P.; Du, X.-H.; Zhong, A.-G.; Xu, D.-Q.; Xu, Z.-Y. Adv. Synth. Catal. 2014, 356, 1753.
      (d) Xia, A.-B.; Zhang, X.-L.; Wang, T.; Du, X.-H.; Xu, D.-Q.; Xu, Z.-Y. New J. Chem. 2015, 39, 5088.
      (e) Xia, A.-B.; Pan, G. J.; Wu, C.; Liu, X.-L.; Zhang, X.-L.; Li, Z.-B.; Du, X.-H.; Xu, D.-Q. Adv. Synth. Catal. 2016, 358, 3155.
      (f) Liu, X.-L.; Zhang, X.-L.; Xia, A.-B.; Guo, Y.-J.; Meng, C.-H.; Xu, D.-Q. Org. Biomol. Chem. 2017, 15, 5126.

    13. [13]

      (a) Rios, R.; Ibrahem, I.; Vesely, J.; Sunden, H.; Córdova, A. Tetrahedron Lett. 2007, 48, 8695.
      (b) Talavera, G.; Reyes, E.; Vicario, J. L.; Carrillo, L.; Uria, U. Adv. Synth. Catal. 2013, 355, 653.

    14. [14]

      Overkleeft, H. S.; van Wiltenburg, J.; Pandit, U. K. Tetrahedron 1994, 50, 4215.  doi: 10.1016/S0040-4020(01)86715-6

    15. [15]

      Kinoshita, M.; Suzuki, Y. Bull. Chem. Soc. Jpn. 1977, 50, 2375.  doi: 10.1246/bcsj.50.2375

    16. [16]

      CCDC 988911 (for 4f) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.

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