Chinese Journal of Organic Chemistry >
Methods and Strategies for the Synthesis of Peduncularine
Received date: 2018-10-09
Revised date: 2018-11-22
Online published: 2018-12-05
Supported by
Project supported by the National Natural Science Foundation of China (No. 21402121) and the Collaborative Innovation Program of Shanghai Institute of Technology (No. XTCX2015-16).
(-)-Peduncularine is the principal alkaloid isolated from Tasmanian shrub Aristotelia peduncularis. Due to its unusual 6-azabicyclo[3.2.1]octane core, the indole alkaloid was received numerous attention from the synthetic community and several innovative synthetic strategies have been developed. In this minireview, the synthetic efforts of peduncularine are summarized as inspiration for future development of medicinally interesting derivatives.
Zhang Yuping , Tian Xuechao , Zhang Yan , Hong Ran , Huang Shahua . Methods and Strategies for the Synthesis of Peduncularine[J]. Chinese Journal of Organic Chemistry, 2019 , 39(1) : 47 -58 . DOI: 10.6023/cjoc201810008
[1] (a) Butler, M. S. J. Nat. Prod. 2004, 67, 2141.
(b) Li, J. W.-H.; Vederas, J. C. Science 2009, 325, 161.
(c) Newman, D. J.; Cragg, G. M. J. Nat. Prod. 2016, 79, 629.
(d) DeCorte, B. L. J. Med. Chem. 2016, 59, 9295.
[2] Lawson, A. D. G.; MacCoss, M.; Heer, J. P. J. Med. Chem. 2018, 61, 4283.
[3] Over, B.; Wetzel, S.; Grütter, C.; Nakai, Y.; Renner, S.; Rauh, D.; Waldmann, H. Nat. Chem. 2013, 5, 21.
[4] Bick, I. R. C.; Bremner, J. B.; Preston, N. W.; Calder, I. C. J. Chem. Soc., Chem. Commun. 1971, 1155.
[5] Ros, H.-P.; Kyburz, R.; Preston, N. W.; Gallagher, R. T.; Bick, I. R. C.; Hesse, M. Helν. Chim. Acta 1979, 62, 481.
[6] Bick, I. R. C.; Hai, M. A.; Preston, N. W. Tetrahedron 1985, 41, 3127.
[7] Klaver, W. J.; Hiemstra, H.; Speckamp, W. N. J. Am. Chem. Soc. 1989, 111, 2588.
[8] Dragar, C.; Bick, I. R. C. Phytochemistry 1992, 31, 3601.
[9] (a) Singh, S. Chem. Rev. 2000, 100, 925.
(b) Pollini, G. P.; Benetti, S.; De Risi, C.; Zanirato, V. Chem. Rev. 2006, 106, 2434.
[10] (a) Carroll, F. I.; Abraham, P.; Parham, K.; Griffith, R. C.; Ahmad, A.; Richard, M. M.; Padilla, F. N.; Witkin, J. M.; Chiang, P. K. J. Med. Chem. 1987, 30, 805.
(b) Carroll, F. I.; Abraham, P.; Mascarella, S. W.; Singh, P.; Moreland, C. G.; Sankar, S. S.; Kwon, Y. W.; Triggle, D. J. J. Med. Chem. 1991, 34, 1436.
[11] Quirante, J.; Vila, X.; Bonjoch, J.; Kozikowski, A. P.; Johnson, K. M. Bioorg. Med. Chem. 2004, 12, 1383.
[12] Holmes, A. B.; Kee, A.; Ladduwahetty, T.; Smith, D. F. J. Chem. Soc., Chem. Commun. 1990, 1412.
[13] Chamberlin, A. R.; Chung, J. Y. L. J. Am. Chem. Soc. 1983, 105, 3653.
[14] (a) Hiemstra, H.; Speckamp, W. N. Tetrahedron Lett. 1983, 24, 1407.
(b) Hiemstra, H.; Klaver, W. J.; Speckamp, W. N. J. Org. Chem. 1984, 49, 1149.
[15] Thomsen, I.; Clausen, K.; Scheibye, S.; Lawesson, S.-O. Org. Synth. 1984, 62, 158.
[16] Robinson, B. Chem. Rev. 1969, 69, 227.
[17] Rigby, J. H.; Meyer, J. H. Synlett 1999, 860.
[18] Rigby, J. H.; Ateeq, H. S.; Charles, N. R.; Henshilwood, J. A.; Short, K. M. Sugathapala, P. M. Tetrahedron 1993, 49, 5495.
[19] McKillop, A.; Hunt, J. D.; Kienzle, F.; Bigham, E.; Taylor, E. C. J. Am. Chem. Soc. 1973, 95, 3635.
[20] Lin, X.; Stien, D.; Weinreb, S. M. Tetrahedron Lett. 2000, 41, 2333.
[21] (a) Hudson, R. F.; Record, K. A. F. J. Chem. Soc., Perkin. 21978, 822.
(b) Lin, X.; Stien, D.; Weinreb, S. M. Org. Lett. 1999, 1, 637.
[22] (a) Washburn, D. G.; Heidebrecht, R. W., Jr.; Martin, S. F. Org. Lett. 2003, 5, 3523.
(b) Martin, S. F. Pure Appl. Chem. 2005, 77, 1207.
[23] (a) Brown, D. S.; Hansson, T.; Ley, S. V. Synlett 1990, 48.
(b) Brown, D. S.; Charreu, P.; Hansson, T.; Ley, S. V. Tetrahedron 1991, 47, 1311.
[24] Roberson, C. W.; Woerpel, K. A. Org. Lett. 2000, 2, 621.
[25] Durst, T.; O'Sullivan, M. J. J. Org. Chem. 1970, 35, 2043.
[26] Roberson, C. W.; Woerpel, K. A. J. Org. Chem. 1999, 64, 1434.
[27] Dubé, D.; Scholte, A. A. Tetrahedron Lett. 1999, 40, 2295.
[28] Groaning, M. D.; Brengel, G. P.; Meyers, A. I. J. Org. Chem. 1998, 63, 5517.
[29] Tamao, K.; Ishida, N.; Tanaka, T.; Kumada, M. Organometallics 1983, 2, 1694.
[30] Roberson, C. W.; Woerpel, K. A. J. Am. Chem. Soc. 2002, 124, 11342.
[31] Shute, R. E.; Rich, D. H. Synthesis 1987, 346.
[32] (a) Hosomi, A.; Sakurai, H. Tetrahedron Lett. 1976, 17, 1295.
(b) Speckamp, W. N.; Moolenaar, M. J. Tetrahedron 2000, 56, 3817.
[33] Roush, W. R.; Gillis, H. R. J. Org. Chem. 1980, 45, 4283.
[34] Abdel-Magid, A. F.; Carson, K. G.; Harris, B. D.; Maryanoff, C. A.; Shah, R. D. J. Org. Chem. 1996, 61, 3849.
[35] Smitrovich, J. H.; Woerpel, K. A. J. Org. Chem. 1996, 61, 6044.
[36] Parikh, J. R.; Doering, W. E. J. Am. Chem. Soc. 1967, 89, 5505.
[37] Cannizzo, L. F.; Grubbs, R. H. J. Org. Chem. 1985, 50, 2386.
[38] Hodgson, D. M.; Shelton, R. E.; Moss, T. A.; Dekhane, M. Org. Lett. 2010, 12, 2834.
[39] Mann, J.; de Almeida Barbosa L.-C. J. Chem. Soc., Perkin Trans. 1 1992, 787.
[40] Davies, H. M. L.; Cao, G. Tetrahedron Lett. 1998, 39, 5943.
[41] Swallen, L. C.; Boord, C. E. J. Am. Chem. Soc. 1930, 52, 651.
[42] Kitamura, M.; Ihara, R.; Uera, Y.; Narasaka, K. Bull. Chem. Soc. Jpn. 2006, 79, 1552.
[43] (a) Uchiyama, K.; Ono, A.; Hayashi, Y.; Narasaka, K. Bull. Chem. Soc. Jpn. 1998, 71, 2945.
(b) Uchiyama, K.; Hayashi, Y.; Narasaka, K. Chem. Lett. 1998, 1261.
[44] Kotsuki, H.; Asao, K.; Ohnishi, H. Bull. Chem. Soc. Jpn. 1984, 57, 3339.
[45] Lenz, G. R.; Woo, C-M.; Hawkins, B. L. J. Org. Chem. 1982, 47, 3049.
[46] (a) Hudrlik, P. F.; Peterson, D. J. Am. Chem. Soc. 1975, 97, 1464.
(b) Johnson, C. R.; Tait, B. D. J. Org. Chem. 1987, 52, 281.
[47] Ragains, J. R.; Winkler, J. D. Org. Lett. 2006, 8, 4437.
[48] (a) Winkler, J. D.; Muller, C. L.; Scott, R. D. J. Am. Chem. Soc. 1988, 110, 4831.
(b) Kwak, Y.-S.; Winkler, J. D. J. Am. Chem. Soc. 2001, 123, 7429.
[49] Comins, D. L; Dehghani. A. Tetrahedron Lett. 1992, 33, 6299.
[50] Jigqjinni, V. B.; Wightman, R. H. Tetrahedron Lett. 1982, 23, 117.
[51] (a) Kyburz, R.; Schöpp, E.; Hesse, M.; Bick, I. R. C. Helv. Chim. Acta 1979, 62, 2539.
(b) Bick, I. R. C.; Hai, M. A.; Preston, N. W. Tetrahedron Lett. 1988, 29, 3355.
(c) Anderson, B. F.; Robertson, G. B.; Avey, P.; Donovan, W. F.; Bick, I. R. C.; Bremner, J. B.; Finney, A. J.T.; Preston, N. W.; Gallagher, R. T.; Russell, G. B. J. Chem. Soc., Chem. Commun. 1975, 511.
(d) Bittner, M.; Silva, M.; Gopalakrishna, E. M.; Watson, W. H.; Zabel, V.; Matlin, S. A.; Sammes, P. G. J. Chem. Soc., Chem. Commun. 1978, 79.
[52] (a) Bick, I. R. C.; Hai, M. A.; Preston, N. W. Heterocycles 1979, 12, 1563.
(b) Saxton, J. E. Nat. Prod. Rep. 1994, 11, 493.
(c) An elegant review on the biomimetic synthesis study of aristotelia alkaloids, see:Borschberg, H.-J. In The Alkaloids: Chemistry and Pharmacology, Vol. 48, Ed.:Cordell, G. A., Elsevier, Academic Press, 1996, Chapter 3, pp. 191~248.
[53] (a) Lovering, F.; Bikker, J.; Humblet, C. J. Med. Chem. 2009, 52, 6752.
(b) Szychowski, J.; Truchon, J.-F.; Bennani, Y. L. J. Med. Chem. 2014, 57, 9292.
(c) Stockdale, T. P.; Williams. C. M. Chem. Soc. Rev. 2015, 44, 7737.
[54] (a) Tamura, O.; Yanagimachi, T.; Kobayashi, T.; Ishibashi, H. Org. Lett. 2001, 3, 2427.
(b) Zhai, H.-B.; Luo, S.-J.; Ye, C.-F.; Ma, Y.-X. J. Org. Chem. 2003, 68, 8268.
(c) Yeung, Y. Y.; Hong, S.-W.; Corey, E. J. J. Am. Chem. Soc. 2006, 128, 6310.
(d) Grainger, R. S.; Welsh, E. J. Angew. Chem., Int. Ed. 2007, 46, 5477.
(e) Campbell, C. L.; Hassler, C.; Ko, S. S.; Voss, M. E.; Guaciaro, M. A.; Carter, P. H.; Cherney, R. J. J. Org. Chem. 2009, 74, 6368.
[55] Kanchupalli, V.; Katukojvala, S. Angew. Chem., Int. Ed. 2018, 57, 5433.
[56] Zhan, Y.-Z.; Liu, T.; Wang, Z.-W. Chem. Eur. J. 2017, 23, 17862.
[57] Mackiewicz, P.; Furstoss, R.; Waegell, B. J. Org. Chem. 1978, 43, 3746.
[58] Liu, T.; Mei, T.-S.; Yu, J.-Q. J. Am. Chem. Soc. 2015, 137, 5871.
[59] Holmes, A. B.; Raithby, P. R.; Thompson, J.; Baxter, A. J. G.; Dixon, J. J. Chem. Soc., Chem. Commun. 1983, 1490.
[60] (a) Callis, D. J.; Thomas, N. F.; Pearson, D. P. J.; Potter, B. V. L. J. Org. Chem. 1996, 61, 4634.
(b) Kumar, P.; Li, P.-H.; Korboukh, I.; Wang, T. L.; Yennawar, H.; Weinreb,S. M. J. Org. Chem. 2011, 76, 2094.
[61] (a) Xie, C.; Luo, J.; Zhang, Y.; Huang, S.-H.; Zhu, L.; Hong, R. Org. Lett. 2018, 20, 2386.
(b) Luo, J.; Xie, C.; Zhang, Y.; Huang, S.-H.; Zhu, L.; Hong, R. Tetrahedron 2018, 74, 5791.
[62] Quirante, J.; Vila, X.; Escolano, C.; Bonjoch, J. J. Org. Chem. 2002, 67, 2323.
[63] Grainger, R. S.; Betou, M.; Male, L.; Pitak, M. B.; Coles, S. J. Org. Lett. 2012, 14, 2234.
[64] Walker, P. D.; Campbell, C. D.; Suleman, A.; Carr, G.; Anderson, E. A. Angew. Chem., Int. Ed. 2013, 52, 9139.
[65] Yeh, M.-C. P.; Chang, Y.-M.; Lin, H.-H. Adv. Synth. Catal. 2017, 359, 2196.
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