Citation: Zhang Yana, Guo Liandong, Xu Jing. Efficient Synthesis of the AC Ring System of Daphnilactone B[J]. Chinese Journal of Organic Chemistry, ;2019, 39(4): 1079-1084. doi: 10.6023/cjoc201811017 shu

Efficient Synthesis of the AC Ring System of Daphnilactone B

  • Corresponding author: Guo Liandong, guold@sustc.edu.cn Xu Jing, xuj@sustc.edu.cn
  • Received Date: 12 November 2018
    Revised Date: 5 December 2018
    Available Online: 21 April 2018

    Fund Project: the Shenzhen Nobel Prize Scientists Laboratory Project C17783101the National Natural Science Foundation of China 21772082Project supported by the National Natural Science Foundation of China (No. 21772082), the Shenzhen Science and Technology Innovation Committee Basic Research Discipline Layout Project and Peacock Technology Innovation (Nos. JCYJ20170817110515599, KQJSCX2017072815423320), the Shenzhen Development and Reform Commission (Discipline Construction Program), the Shenzhen Peacock Plan (No. KQTD20150717103157174) and the Shenzhen Nobel Prize Scientists Laboratory Project (No. C17783101)the Shenzhen Science and Technology Innovation Committee Basic Research Discipline Layout Project and Peacock Technology Innovation JCYJ20170817110515599the Shenzhen Peacock Plan KQTD20150717103157174the Shenzhen Science and Technology Innovation Committee Basic Research Discipline Layout Project and Peacock Technology Innovation KQJSCX2017072815423320

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  • The synthesis of the AC ring moiety of daphnilactone B has been achieved through an efficient Diels-Alder reaction and Au-catalyzed Conia-ene reaction in seven steps with 30% overall yield.Our strategies paved the way to the total synthesis of various daphnilactone B-type Daphniphyllum alkaloids.
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    1. [1]

    2. [2]

      Sasaki, K.; Hirata, Y.Tetrahedron Lett.1972, 13, 1891.  doi: 10.1016/S0040-4039(01)84744-4

    3. [3]

      Yamamura, S.; Terada, Y.Chem.Lett.1976, 5, 1381.  doi: 10.1246/cl.1976.1381

    4. [4]

      Kong, N.-C.; He, H.-P.; Wang, Y.-H.; Mu, S.-Z.; Di, Y.-T.; Hao, X.-J.J.Nat.Prod.2007, 70, 1348.  doi: 10.1021/np0700220

    5. [5]

      Zhan, Z.-J.; Zhang, C.-R.; Yue, J.-M.Tetrahedron 2005, 61, 11038.  doi: 10.1016/j.tet.2005.03.146

    6. [6]

      For synthetic studies published after Ref.[1c], see:
      (a) Li, J.L.; Shi, H.W.; Wang, Q.; Chai, Y.H.; Yang, J.Org.Lett.2017, 19, 1497.
      (b) Boissarie, P.; Bélanger, G.Org.Lett.2017, 19, 3739.
      (c) Liu, Y.M.; Li, F.; Wang, Q.; Yang, J.Tetrahedron 2017, 73, 6381.
      (d) Shao, H.; Bao, W.; Jing, Z.-R.; Wang, Y.-P.; Zhang, F.-M.; Wang, S.-H.; Tu, Y.-Q.Org.Lett.2017, 19, 4648.
      (e) Lopez, A.M.; Ibrahim, A.A.; Rosenhauer, G.J.; Sirinimal, H.S.; Stockdill, J.L.Org.Lett.2018, 20, 2216.
      (f) Sasano, Y.; Koyama, J.; Yoshikawa, K.; Kanoh, N.; Kwon, E.; Iwabuchi, Y.Org.Lett.2018, 20, 3053.
      (g) Yamada, R.; Fukuyama, T.; Yokoshima, S.Org.Lett.2018, 20, 4504.
      (h) Li, Y.; Dong, Q.; Xie, Q.; Tang, P.; Zhang, M.; Qin, Y.Org.Lett.2018, 20, 5053.
      (i) Qiu, Y.; Zhong, J.; Du, S.; Gao, S.Chem.Commun.2018, 54, 5554.
      (j) Kitabayashi, Y.; Fukuyama, T.; Yokoshima, S.Org.Biomol.Chem.2018, 16, 3556.
      (k) Mo, X.-F.; Li, Y.-F.; Sun, M.-H.; Dong, Q.-Y.; Xie, Q.-X.; Tang, P.; Xue, F.; Qin, Y.Tetrahedron Lett.2018, 59, 1999.
      (l) Cox, J.B.; Wood, J.L.Tetrahedron 2018, 74, 4539.

    7. [7]

      (a) Heathcock, C.H.; Davidsen, S.K; Mills, S.; Sanner, M.A.J.Am.Chem.Soc.1986, 108, 5650.
      (b) Ruggeri, R.B.; Hansen, M.M.; Heathcock, C.H.J.Am.Chem.Soc.1988, 110, 8734.
      (c) Ruggeri, R.B.; McClure, K.F.; Heathcock, C.H.J.Am.Chem.Soc.1989, 111, 1530.
      (d) Ruggeri, R.B.; Heathcock, C.H.J.Org.Chem.1990, 55, 3714.
      (e) Stafford, J.A.; Heathcock, C.H.J.Org.Chem.1990, 55, 5433.
      (f) Piettre, S.; Heathcock, C.H.Science 1990, 248, 1532.
      (g) Heathcock, C.H.; Stafford, J.A.; Clark, D.L.J.Org.Chem.1992, 57, 2575.
      (h) Heathcock, C.H.Angew.Chem., Int.Ed.Engl.1992, 31, 665.
      (i) Heathcock, C.H.; Joe, D.J.Org.Chem.1995, 60, 1131.
      (j) Heathcock, C.H.; Kath, J.C.; Ruggeri, R.B.J.Org.Chem.1995, 60, 1120.
      (k) Heathcock, C.H.Proc.Natl.Acad.Sci.U.S.A. 1996, 93, 14323.
      (l) Wallace, G.A.; Heathcock, C.H.J.Org.Chem.2001, 66, 450.

    8. [8]

      Weiss, M.E.; Carreira, E.M.Angew.Chem., Int.Ed.2011, 50, 11501.  doi: 10.1002/anie.v50.48

    9. [9]

      (a) Shvartsbart, A.; Smith, A.B.Ⅲ J.Am.Chem.Soc.2014, 136, 870.
      (b) Shvartsbart, A.; Smith, A.B.Ⅲ J.Am.Chem.Soc.2015, 137, 3510.(a) Shvartsbart, A.; Smith, A.B.Ⅲ J.Am.Chem.Soc.2014, 136, 870.
      (b) Shvartsbart, A.; Smith, A.B.Ⅲ J.Am.Chem.Soc.2015, 137, 3510.

    10. [10]

      (a) Lu, Z.; Li, Y.; Deng, J.; Li, A.Nat.Chem.2013, 5, 679.
      (b) Xiong, X.; Li, Y.; Lu, Z.; Wan, M.; Deng, J.; Wu, S.; Shao, H.; Li, A.Chem.Commun.2014, 50, 5294.
      (c) Li, J.; Zhang, W.; Zhang, F.; Chen, Y.; Li, A.J.Am.Chem.Soc.2017, 139, 14893.
      (d) Chen, Y.; Zhang, W.; Ren, L.; Li, J.; Li, A.Angew.Chem., Int.Ed.2018, 57, 952.
      (e) Zhang, W.; Ding, M.; Li, J.; Guo, Z.; Lu, M.; Chen, Y.; Liu, L.; Shen, Y.-H.; Li, A.J.Am.Chem.Soc.2018, 140, 4227.

    11. [11]

      For the total synthesis of a putative natural Daphniphyllum alkaloid isodaphlongamine H: Chattopadhyay, A.K.; Ly, V.L.; Jakkepally, S.; Berger, G.; Hanessian, S.Angew.Chem., Int.Ed.2016, 55, 2577.

    12. [12]

      Yamada, R.; Adachi, Y.; Yokoshima, S.; Fukuyama, T.Angew.Chem., Int.Ed.2016, 55, 6067.  doi: 10.1002/anie.201601958

    13. [13]

      Chen, X.; Zhang, H.-J.; Yang, X.; Lv, H.; Shao, X.; Tao, C.; Wang, H.; Cheng, B.; Li, Y.; Guo, J.; Zhang, J.; Zhai, H.Angew.Chem., Int.Ed.2018, 57, 947.  doi: 10.1002/anie.201709762

    14. [14]

      Shi, H.; Michaelides, I.N.; Darses, B.; Jakubec, P.; Nguyen, Q.N.N.; Paton, R.S.; Dixon, D.J.J.Am.Chem.Soc.2017, 139, 17755.  doi: 10.1021/jacs.7b10956

    15. [15]

      Denmark, S.E.; Baiazitov, R.Y.J.Org.Chem.2006, 71, 593.  doi: 10.1021/jo052001l

    16. [16]

      (a) Denmark, S.E.; Baiazitov, R.Y.; Nguyen, S.T.Tetrahedron 2009, 65, 6535.
      (b) Denmark, S.E.; Nguyen, S.T.; Baiazitov, R.Y.Heterocycles 2008, 76, 143.

    17. [17]

      Coldham, I.; Burrell, A.J.M.; Guerrand, H.D.S.; Oram, N.Org.Lett.2011, 13, 1267.  doi: 10.1021/ol102961x

    18. [18]

      (a) Staben, S.T.; Kennedy-Smith, J.J.; Huang, D.; Corkey, B.K.; Lalonde, R.L.; Toste, F.D.Angew.Chem., Int.Ed.2006, 45, 5991.
      (b) Huwyler, N.; Carreira, E.M.Angew.Chem., Int.Ed.2012, 51, 13066. For a Conia-ene reaction catalyzed by Rh, see: :
      (c) Long, R.; Huang, J.; Shao, W.; Liu, S.; Lan, Y.; Gong, J.; Yang, Z.Nat.Commun.2014, 5, 5707.

    19. [19]

      Kozmin, S.A.; Rawal, V.H.J.Org.Chem.1997, 62, 5252.  doi: 10.1021/jo970438q

    20. [20]

      Terrasson, V.; van der Lee, A.; Marcia de Figueiredo, R.; Campagne, J.M.Chem.-Eur.J.2010, 16, 7875.  doi: 10.1002/chem.201000334

    21. [21]

      Zhang, P.-P.; Yan, Z.M.; Li, Y.-H.; Gong, J.-X.; Yang, Z.J.Am.Chem.Soc.2017, 139, 13989.  doi: 10.1021/jacs.7b07388

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