Citation: Huang Guobao, Chen Zhilin, Wei Xiansheng, Chen Yu, Li Xiuying, Zhong Hui, Tan Mingxiong. Recent Progress on the Construction and Function of Macrocyclic Compounds Containing Hydrogen Bond Donors[J]. Chinese Journal of Organic Chemistry, ;2020, 40(3): 614-624. doi: 10.6023/cjoc201909029 shu

Recent Progress on the Construction and Function of Macrocyclic Compounds Containing Hydrogen Bond Donors

Huang Guobao ^a,† ,
Chen Zhilin ^a,† ,
Wei Xiansheng ^a ,
Chen Yu ^a ,
Li Xiuying ^a ,
Zhong Hui ^b,, ,
Tan Mingxiong ^a,,

a.
Guangxi Key Laboratory of Agricultural Resources Chemistry and Biotechnology, College of Chemistry and Food Science, Yulin Normal University, Yulin, Guangxi 537000
b.
School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing 211100

Corresponding author: Zhong Hui, lxya8401@163.com Tan Mingxiong, tanmx00@163.com
Received Date: 18 September 2019
Revised Date: 31 October 2019
Available Online: 2 December 2019
Fund Project: the Yulin Normal University Research Grant 201810606010the National Natural Science Foundation of China 21961042the Yulin Normal University Research Grant 2018YJKY36the Natural Science Foundation of Guangxi Province 2018GXNSFAA294064Project supported by the National Natural Science Foundation of China (No. 21961042), the Natural Science Foundation of Guangxi Province (No. 2018GXNSFAA294064) and the Yulin Normal University Research Grant (Nos. 2018YJKY36, 201810606010)

Figures(14)

Because of the N-H group structure in the macrocyclic compound containing hydrogen bond Donors, it can provide additional intermolecular forces in the host-guest chemistry, and this character is widely used in the molecular recognition, self-assembly, supramolecular catalysis and other fields. The recent progress on the synthetic methods of macrocyclic compounds based on (thio) urea, amide and its molecular recognition in 2010~2019 are summarized. It is hoped that this review can be referred to synthesis and applications of this kind of macrocyclic compounds.
- hydrogen bond donor group,
- macrocyclic compounds,
- synthesis,
- molecular recognition
1. [1]
2. [2]
  Pedersen, C. J. J. Am. Chem. Soc. 1967, 89, 7017. doi: 10.1021/ja01002a035
3. [3]
  Huang, G.-B.; Jiang, W. Prog. Chem. 2015, 27, 744 (in Chinese).
4. [4]
  (a) Zheng, B.; Wang, F.; Dong, S.-Y.; Huang, F.-H. Chem. Soc. Rev. 2012, 5, 1621.
  (b) Cheng, H.-B.; Zhang, H.-Y.; Liu, Y. J. Am. Chem. Soc. 2013, 135, 10190.
5. [5]
  (a) Liu, Y.; Chen, Y. Acc. Chem. Res. 2006, 10, 681.
  (b) Chen, Y.; Liu, Y. Chem. Soc. Rev. 2010, 39, 495.
6. [6]
  (a) Guo, D.-S.; Wang, K.; Liu, Y. J. Inclusion Phenom. Macrocyclic Chem. 2008, 1-2, 1.
  (b) Guo, D.-S.; Liu, Y. Chem. Soc. Rev. 2012, 41, 5907.
7. [7]
  (a) Xue, M.; Yang, Y.; Chi, X.; Zhang, Z.; Huang, F. Acc. Chem. Res. 2012, 45, 1294.
  (b) Cragg, P. J.; Sharma, K. Chem. Soc. Rev. 2012, 41, 597.
  (c) Ogoshi, T.; Yamagishi, T.-A. Eur. J. Org. Chem. 2013, 15, 2961.
  (d) Zhang, H.; Zhao, Y. Chem.-Eur. J. 2013, 19, 16862.
  (e) Wang, M.-X. Chem. Commun. 2008, 4541.
  (f) Guo, Q.-H.; Fu, Z.-D.; Zhao, L.; Wang, M.-X. Angew. Chem., Int. Ed. 2014, 53, 13548.
  (g) Wang, M.-X. Acc. Chem. Res. 2012, 45, 182.
  (h) Chen, H.; Fan, J.; Hu, X.; Ma, J.; Wang, S.; Li, J.; Yu, Y.; Jia, X.; Li, C. Chem. Sci. 2015, 6, 197.
  (i) Tian, X. H.; Chen, C. F. Org. Lett. 2010, 12, 524.
  (j) Xue, M.; Chen, C. F. Org. Lett. 2009, 11, 5294.
  (k) Wang, J. H.; Feng, H. T.; Zheng, Y. S. Chem. Commun. 2014, 50, 11407.
  (l) Chun, Y.; Singh, N. J.; Hwang, I. C.; Lee, J. W.; Yu, S.-U.; Kim, K.-S. Nat. Commun. 2013, 4, 1797.
  (m) Lee, S.; Chen, C.-H.; Flood, A.-H. Nat. Chem. 2013, 5, 704.
8. [8]
  Shimizu, L. S.; Smith, M. D.; Hughes, A. D.; Shimizu, K. D. Chem. Commun. 2001, 1592.
9. [9]
  (a) Shimizu, L. S.; Hughes, A. D.; Smith, M. D.; Davis, M. J.; Zhang, P.; Loye zur, H.; Shimizu, K. D. J. Am. Chem. Soc. 2003, 125, 14972.
  (b) Yang, J.; Dewal, M. B.; Shimizu, L. S. J. Am. Chem. Soc. 2006, 128, 8122.
  (c) Yang, J.; Dewal, M. B.; Profeta, S.; Smith, M. D.; Li, Y.; Shimizu, L. S. J. Am. Chem. Soc. 2008, 130, 612.
  (d) Dewal, M. B.; Xu, Y.; Yang, J.; Mohammed, F.; Smith, M. D.; Shimizu, L. S. Chem. Commun. 2008, 3909.
  (e) Yang, J.; Dewal, M. B.; Sobransingh, D.; Smith, M. D.; Xu, Y.; Shimizu, L. S. J. Org. Chem. 2009, 74, 102.
  (f) Xu, Y.; Smith, M. D.; Krause, J.; Shimizu, L. S. J. Org. Chem. 2009, 74, 4874.
  (f) Roy, K.; Wang, C.; Smith, M.-D.; Pellechia, P.; Shimizu, L. S. J. Org. Chem. 2010, 75, 5453.
10. [10]
  (a) Meshcheryakov, D.; Arnaud-Neu, F.; Böhmer, V.; Bolte, M.; Cavaleri, J.; Hubscher-Bruder, V.; Thondorf, I.; Weener, S. Org. Biomol. Chem. 2008, 6, 3244.
  (b) Meshcheryakov, D.; Böhmer, V.; Bolte, M.; Hubscher-Bruder, V.; Arnaud-Neu, F. Chem. Eur. J. 2009, 15, 4811.
11. [11]
  Dawn, S.; Dewal, M. B.; Sobransingh, D.; Paderes, M. C.; Wibowo, A.; Smith, M.; Krause, J.; Pellechia, P.; Shimizu, L. S. J. Am. Chem. Soc. 2011, 133, 7025. doi: 10.1021/ja110779h
12. [12]
  Roy, K.; Wang, C.; Smith, M. D.; Dewal, M. B.; Wibowo, A. C.; Brown, J. C.; Ma, S.; Shimizu, L. S. Chem. Commun. 2011, 47, 277. doi: 10.1039/C0CC01952F
13. [13]
  Geer, M. F.; Smith, M. D.; Shimizu, L. S. CrystEngComm 2011, 13, 3665. doi: 10.1039/c1ce05207a
14. [14]
  Roy, K.; Wibowo, A.; Pellechia, P.; Ma, S.; Geer, M.; Shimizu, L. S. Chem. Mater. 2012, 24, 4773 doi: 10.1021/cm302658q
15. [15]
  Geer, M. F.; Walla, M.; Solntsev, K.; Strassert, C.; Shimizu, L. S. J. Org. Chem. 2013, 78, 5568. doi: 10.1021/jo400685u
16. [16]
  Xiao, T.; Li, S.; Zhang, X.; Lin, C.; Wang, L. Y. Chin. J. Chem. 2013, 31, 627. doi: 10.1002/cjoc.201300246
17. [17]
  Zhang, D. S.; Chen, J. P.; Zeng, Y.; Yu, T. J.; Li, Y. Chin. J. Org. Chem. 2013, 33, 110 (in Chinese).
18. [18]
  Kretschemer, C.; Dittmann, G.; Beck, J. Beilstein J. Org. Chem. 2014, 10, 1834. doi: 10.3762/bjoc.10.193
19. [19]
  Huang, G. B.; He, Z.; Cai, C.; Pan, F.; Yang, D.; Rissanen, K.; Jiang, W. Chem. Commun. 2015, 51, 15490. doi: 10.1039/C5CC06768E
20. [20]
  Huang, G. B.; Valkonen, A.; Rissanen, K.; Jiang, W. Chem. Commun. 2016, 52, 9078. doi: 10.1039/C6CC00349D
21. [21]
  Huang, G. B.; Liu, V.; Valkonen, A.; Yao, H.; Rissanen, K.; Jiang, W. Chin. Chem. Lett. 2018, 29, 91. doi: 10.1016/j.cclet.2017.07.005
22. [22]
  (a) Kondo, S.; Sonoda, H.; Katsu, T.; Unno, M. Sens. Actuators, B 2011, 160, 684.
  (b) Satake, A.; Ishizawa, Y.; Katagiri, H.; Kondo, S. J. Org. Chem. 2016, 81, 9848.
23. [23]
  Osawa, K.; Tagaya, H.; Kondo, S. J. Org. Chem. 2019, 84, 6623. doi: 10.1021/acs.joc.9b00073
24. [24]
  Tromans, R.; Carter, T.; Chabanne, T.; Crump, M.; Li, H.; Matlock, J.; Orchard, M.; Davis, A. P. Nat. Chem. 2019, 11, 52.
25. [25]
  (a) Shorthill, B. J.; Avetta, C. T.; Glass, T. E. J. Am. Chem. Soc. 2004, 126, 12732.
  (b) Sharma, S. K.; Upreti, S.; Gupta, R. Eur. J. Inorg. Chem. 2007, 3247.
  (c) Gasparrini, F.; Pierini, M.; Villani, C.; Filippi, A.; Speranza, M. J. Am. Chem. Soc. 2008, 130, 522.
  (d) Shang, X. F.; Lin, H.; Cai, Z. S.; Lin, H. K. J. Heterocycl. Chem. 2008, 45, 1329.
  (d) Ghorai, A.; Gayen, A.; Kulsi, G.; Padmanaban, E.; Laskar, A.; Achari, B.; Mukhopadhyay, C.; Chattopadhyay, P. Org. Lett. 2011, 13, 5512.
26. [26]
  (a) Fuller, A. M.; Leigh, D. A.; Lusby, P. J.; Oswald, I. D. H.; Parsons, S.; Walker, D. B. Angew. Chem. 2004, 116, 4004.
  (b) Leigh, D. A.; Venturini, A.; Wilson, A. J.; Wong, J. K. Y.; Zerbetto, F. Chem.-Eur. J. 2004, 10, 4960.
  (c) Fuller, A. M.; Leigh, D. A.; Lusby, P. J.; Oswald, I. D. H.; Parsons, S.; Walker, D. B. J. Am. Chem. Soc. 2005, 137, 12612.
  (d) Crowley, J. D.; Leigh, D. A.; Lusby, P. J.; McBurney, R. T.; Perret-Aebi, L. E.; Petzold, C.; Slawin, A. M. Z.; Symes, M. D. J. Am. Chem. Soc. 2007, 129, 15085.
  (e) Barrell, M. J.; Leigh, D. A.; Lusby, P. J.; Slawin, A. M. Z. Angew. Chem., Int. Ed. 2008, 47, 8036.
  (f) Altieri, A.; Aucagne, V.; Carrillo, R.; Clarkson, G.; D'Souza, D. M.; Dunnet, J.; Leigh, D. A.; Mullen, K. M. Chem. Sci. 2011, 2, 1922.
27. [27]
  (a) Klein, E.; Ferrand, Y.; Auty, E. K.; Davis, A. P. Chem. Commun. 2007, 2390.
  (b) Ferrand, Y.; Crump, M. P.; Davis, A. P. Science 2007, 318, 619.
  (c) Klein, E.; Ferrand, Y.; Barwell, N. P.; Davis, A. P. Angew. Chem., Int. Ed. 2008, 48, 2693.
  (d) Challinor, L.; Klein, E.; Davis, A. P. Synlett 2008, 14, 2137.
28. [28]
  Qin, B.; Chen, X. Y.; Fang, X.; Shu, Y. Y.; Yip, Y. K.; Yan, Y.; Pan, S. Y.; Ong, W. Q.; Ren, C. L.; Su, H. B.; Zeng, H. Q. Org. Lett. 2008, 10, 5127. doi: 10.1021/ol801980h
29. [29]
  Qin, B.; Ren, C.; Ye, R.; Sun, C.; Chalid, K.; Chen, X.; Li, Z.; Xue, F.; Su, H.; Chass, G.; Zeng, H. Q. J. Am. Chem. Soc. 2010, 132, 9564. doi: 10.1021/ja1035804
30. [30]
  (a) Helsel, A. J.; Brown, A. L.; Yamato, K.; Feng, W.; Yuan, L. H.; Clements, A.; Harding, S. V.; Szabo, G.; Shao, Z. F.; Gong, B. J. Am. Chem. Soc. 2008, 130, 15784.
  (b) Wang, X.; Liu, R.; Sathyamoorthy, B.; Yamato, K.; Liang, G.; Shen, L.; Ma, S.; Sukumaran, D.; Szyperski, T.; Fang, W.; He, L.; Chen, X.; Gong, B. J. Am. Chem. Soc. 2015, 137, 5879.
31. [31]
  Yang, Y.; Feng, W.; Hu, J.; Zou, S.; Gao, R.; Yamato, K.; Kline, M.; Cai, Z.; Gao, Y.; Wang, Y.; Li, Y.; Yang, Y.; Yuan, L.; Zeng, X.; Gong, B. J. Am. Chem. Soc. 2011, 133, 18590. doi: 10.1021/ja208548b
32. [32]
  (a) Ferrand, Y.; Klein, E.; Barwell, N. P.; Crump, M. P.; J. Vicent, J. C.; Boons, G.-J.; Ingale, S.; Davis, A. P. Angew. Chem., Int. Ed. 2009, 49, 1775.
  (b) Davis, A. P. Org. Biomol. Chem. 2009, 7, 3629.
  (c) Barwell, N. P.; Crump, M. P.; Davis, A. P. Angew. Chem., Int. Ed. 2009, 48, 7363.
33. [33]
  Barwell, N. P.; Davis, A. P. J. Org. Chem. 2011, 76, 6548. doi: 10.1021/jo200755z
34. [34]
  (a) Sookcharoenpinyo, B.; Klein, E.; Ferrand, Y.; Walker, B.; Brotherhood, P.; Ke, C.; Crump, M. P.; Davis, A. P. Angew. Chem., Int. Ed. 2012, 51, 4586.
  (b) Ke, C.; Destecroix, H.; Crump, M. P.; Davis, A. P. Nat. Chem. 2012, 4, 718.
  (c) Howgego, J.; Butts, C.; Crump, M. P.; Davis, A. P. Chem. Commun. 2013, 49, 3110.
  (d) Destecroix, H.; Renney, C.; Mooibroek, T.; Carter, T.; Stewart, P.; Crump, M. P.; Davis, A. P. Angew. Chem. Int. Ed. 2015, 54, 2057.
  (e) Rios, P.; Carter, T.; Mooibroek, T.; Crump, M. P.; Lisbjerg, M.; Pittelkow, M.; Supekar, N.; Boons, G.; Davis, A. P. Angew. Chem., Int. Ed. 2016, 55, 3387.
  (f) Carter, T.; Mooibroek, T.; Stewart, P.; Crump, M. P.; Galan, M.; Davis, A. P. Angew. Chem., Int. Ed. 2016, 55, 9311.
  (g) Mandal, P.; Kauffmann, B.; Destecroix, H.; Ferrand, Y.; Davis, A. P.; Huc, I. Chem. Commun. 2016, 52, 9355.
  (h) Rios, P.; Mooibroek, T.; Carter, T.; Willams, C.; Wilson, M.; Crump, M. P.; Davis, A. P. Chem. Sci. 2017, 8, 4056.
35. [35]
  Chen, M. J.; Han, S. J.; Jiang, L. S.; Zhou, S. G.; Jiang, F.; Xu, Z. K.; Liang, J. D.; Zhang, S. H. Chem. Commun. 2010, 46, 3932. doi: 10.1039/c003118f
36. [36]
  Yang, D. K.; Zeng, Z. J.; Chen, M. J.; Pan, S. W.; Yang, Y.; Li, M.; Lei, C. Y.; Jiang. L. S. Acta Chim. Sinica 2012, 74, 1385 (in Chinese).
37. [37]
  Wang, D.; You, L.; Wang, J.; Wang, H.; Zhang, D.; Li, Z. T. Tetrahedron Lett. 2013, 54, 6967. doi: 10.1016/j.tetlet.2013.10.064
38. [38]
  Chen, Y.; Wang, L.; Zhang, L.; Zhu, J.; Wang, H.; Zhang, D.; Li, Z. T. Tetrahedron 2014, 70, 5483. doi: 10.1016/j.tet.2014.06.113
39. [39]
  Huang, G.; Wang, S.; Ke, H.; Yang, L.; Jiang, W. J. Am. Chem. Soc. 2016, 138, 14550 doi: 10.1021/jacs.6b09472
40. [40]
  Martí-Centelles, V.; Burguete, M. I.; Luis, S. J. Org. Chem. 2016, 81, 2143. doi: 10.1021/acs.joc.5b02676
41. [41]
  Mao, L.; Pan, W.; Fu, Y.; Chen, L.; Xu, M.; Ren, Y.; Feng, W.; Yuan, L. Org. Lett. 2017, 19, 18. doi: 10.1021/acs.orglett.6b03125
42. [42]
  Wang, F. F.; Ou, M.; Deng, Y. X.; Ran, X.; Zhang, Q. L.; Zhu, B. X. Chin. J. Org. Chem. 2014, 34, 334 (in Chinese).
43. [43]
  Wei, X. K.; Gu, J. C.; Liu, X. L.; Huang, C.; Zhu, B. X. Chin. J. Org. Chem. 2018, 38, 3386 (in Chinese).
44. [44]
  (a) Johnston, A. G.; Leigh, D. A.; Pritchard, R. J.; Deegan, M. D. Angew. Chem., Int. Ed. Engl. 1995, 34, 1209.
  (b) Leigh, D. A.; Venturini, A.; Wilson, A. J.; Wong, J. K. Y.; Zerbetto, F. Chem.-Eur. J. 2004, 10, 4960.
45. [45]
  María, D.; Claramunt, R.; Torralba, M.; Torres, M.; Elguero, J. Tetrahedron Lett. 2019, 60, 1206. doi: 10.1016/j.tetlet.2019.03.066
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