Citation: Guo Xiao, Wang Yazhou, Chen Jie, Li Gongqiang, Xia Ji-Bao. Recent Advances of CO₂ Fixation via Asymmetric Catalysis for the Direct Synthesis of Optically Active Small Molecules[J]. Chinese Journal of Organic Chemistry, ;2020, 40(8): 2208-2220. doi: 10.6023/cjoc202002032 shu

Recent Advances of CO₂ Fixation via Asymmetric Catalysis for the Direct Synthesis of Optically Active Small Molecules

Guo Xiao ^a ,
Wang Yazhou ^b ,
Chen Jie ^b,, ,
Li Gongqiang ^a,, ,
Xia Ji-Bao ^b,,

a.
Key Laboratory of Flexible Electronic&Institute of Advanced Materials, Jiangsu National Synergistic Innovation Center for Advanced Materials, Nanjing Tech University, Nanjing 211816
b.
State Key Laboratory for Oxo Synthesis and Selective Oxidation, Center for Excellence in Molecular Synthesis, Suzhou Research Institute of LICP, Lanzhou Institute of Chemical Physics(LICP), Chinese Academy of Sciences, Lanzhou 730000

Corresponding author: Chen Jie, chenjie318827@hotmail.com Li Gongqiang, iamgqli@njtech.edu.cn Xia Ji-Bao, jibaoxia@licp.cas.cn
Received Date: 24 February 2020
Revised Date: 8 May 2020
Available Online: 15 May 2020
Fund Project: the National Natural Science Foundation of China 21772208the National Natural Science Foundation of China 21702212the Key Research Program of Frontier Sciences of Chinese Academy of Sciences QYZDJSSW-SLH051Project supported by the National Natural Science Foundation of China (Nos. 21702212, 21772208) and the Key Research Program of Frontier Sciences of Chinese Academy of Sciences (No. QYZDJSSW-SLH051)

Figures(28)

Industrial processes of fixing carbon dioxide (CO₂) lag far behind the carbon emission generated by human activity. Since CO₂ is an abundant, non-toxic, and cost-effective one carbon source, it is highly desirable to develop methodologies on converting CO₂ into valuable products for sustainable purpose. Based on the mechanistic insight of CO₂ activation by transition-metal catalyst and organocatalyst, a variety of efficient asymmetric CO₂ chemical fixation processes have been developed in recent years. This review discusses the advances of enantioselective synthesis of small molecules by asymmetric catalytic reactions with CO₂. The interaction between catalyst, CO₂ and substrate has been elaborated aiming to inspire the design of new catalytic systems for asymmetric CO₂ transformation.
- carbon dioxide,
- asymmetric catalysis,
- enantioselectivity,
- carboxylation,
- cyclization
1. [1]
  Scott, A. Chem. Eng. News 2015, 93, 10. doi: 10.1021/cen-09237-bus1
2. [2]
  Aresta, M. Carbon Dioxide as Chemical Feedstock, Wiley-VCH, Weinheim, 2010.
3. [3]
  Liu, Q.; Wu, L.; Jackstell, R.; Beller, M. Nat. Commun. 2015, 6, 5933. doi: 10.1038/ncomms6933
4. [4]
  Fiorani, G.; Guo, W.; Kleij, A.-W. Green Chem. 2015, 17, 1375. doi: 10.1039/C4GC01959H
5. [5]
  Yu, B.; He, L.-N. ChemSusChem 2015, 8, 52. doi: 10.1002/cssc.201402837
6. [6]
  Maeda, C.; Miyazaki, Y.; Ema, T. Catal. Sci. Technol. 2014, 4, 1482. doi: 10.1039/c3cy00993a
7. [7]
  Tlili, A.; Frogneux, X.; Blondiaux, E.; Cantat, T. Angew. Chem., Int. Ed. 2014, 53, 2543. doi: 10.1002/anie.201310337
8. [8]
  Yuan, G.; Qi, C.; Wu, W.; Jiang, H. Curr. Opin. Green Sust. Chem. 2017, 3, 22. doi: 10.1016/j.cogsc.2017.03.003
9. [9]
  Zhang, W.; Zhang, N.; Guo, C.-X.; Lü, X. Chin. J. Org. Chem. 2017, 37, 1309(in Chinese).
10. [10]
  Zhang, Z.; Ju, T.; Ye, J.-H.; Yu, D.-G. Synlett 2017, 28, 741. doi: 10.1055/s-0036-1588403
11. [11]
  Gui, Y.-Y.; Zhou, W.-J.; Ye, J.-H.; Yu, D.-G. ChemSusChem 2017, 10, 1337. doi: 10.1002/cssc.201700205
12. [12]
  Cao, Y.; He, X.; Wang, N.; Li, H.-R.; He, L.-N. Chin. J. Chem. 2018, 36, 644. doi: 10.1002/cjoc.201700742
13. [13]
  Zhao, Y., Liu, Z.-M. Chin. J. Chem. 2018, 36, 455 doi: 10.1002/cjoc.201800014
14. [14]
  Hu, J.; Liu, H.; Han, B. Sci. China Chem. 2018, 61, 1486. doi: 10.1007/s11426-018-9396-3
15. [15]
  Tan, F.; Yin, G. Chin. J. Chem. 2018, 36, 545. doi: 10.1002/cjoc.201800011
16. [16]
  Zhang, Z.; Gong, L.; Zhou, X.-Y.; Yan, S.-S.; Li, J.; Yu, D.-G. Acta Chim. Sinica 2019, 77, 783(in Chinese).
17. [17]
  Cheng, L.; Xie, J.-H. Chin. J. Org. Chem. 2020, 40, 247(in Chinese).
18. [18]
  Kolbe, H. Justus Liebigs Ann. Chem. 1860, 113, 125. doi: 10.1002/jlac.18601130120
19. [19]
  Lindsey, A.-S.; Jeskey, H. Chem. Rev. 1957, 57, 583. doi: 10.1021/cr50016a001
20. [20]
  Luo, J.; Preciado, S.; Xia, P.; Larrosa, L. Chem.-Eur. J. 2016, 22, 6798. doi: 10.1002/chem.201601114
21. [21]
  Zhang, W.-Z.; Li, H.; Zeng, Y.; Tao, X.; Lu, X. Chin. J. Chem. 2018, 36, 112. doi: 10.1002/cjoc.201700581
22. [22]
  Sakakura, T.; Choi, J.-C.; Yasuda, H. Chem. Rev. 2007, 107, 2365. doi: 10.1021/cr068357u
23. [23]
  White, J.-L.; Baruch, M.-F.; Pander Ⅲ, J.-E.; Hu, Y.-I.; Fortmeyer, C.; Park, J.-E.; Zhang, T.; Liao, K.; Gu, J.; Yan, Y.; Shaw, T.-W.; Abelev, E.; Bocarsly, A.-B. Chem. Rev. 2015, 115, 12888. doi: 10.1021/acs.chemrev.5b00370
24. [24]
  Wang, J.-L.; Miao, C.-X.; Dou, X.-Y.; Gao, J.; He, L.-N. Curr. Org. Chem. 2011, 15, 621. doi: 10.2174/138527211794518952
25. [25]
  Tlili, A.; Blondiaux, E.; Frogneux, X.; Cantat, T. Green Chem. 2015, 17, 157. doi: 10.1039/C4GC01614A
26. [26]
  Li, Y.; Cui, X.; Dong, K.; Junge, K.; Beller, M. ACS Catal. 2017, 7, 1077. doi: 10.1021/acscatal.6b02715
27. [27]
  Liu, M.; Qin, T.; Zhang, Q.; Fang, C.; Fu, Y.; Lin, B.-L. Sci. China Chem. 2015, 58, 1524. doi: 10.1007/s11426-015-5405-y
28. [28]
  Zhang, L.; Zhao, Z.-J.; Gong, J. Angew. Chem., Int. Ed. 2017, 56, 11326. doi: 10.1002/anie.201612214
29. [29]
  Yu, D.; Teong, S.-P.; Zhang, Y. Coord. Chem. Rev. 2015, 293-294, 279. doi: 10.1016/j.ccr.2014.09.002
30. [30]
  Liu, A.-H.; Yu, B.; He, L.-N. Greenhouse Gas Sci. Technol. 2015, 5, 17. doi: 10.1002/ghg.1461
31. [31]
  Yeung, C.-S.; Dong, V.-M.; Top. Catal. 2014, 57, 1342. doi: 10.1007/s11244-014-0301-9
32. [32]
  Zhang, W.; Lu, X. Chin. J. Catal. 2012, 33, 745. doi: 10.1016/S1872-2067(11)60390-2
33. [33]
  Tsuji, Y.; Fujihara, T. Chem. Commun. 2012, 48, 9956. doi: 10.1039/c2cc33848c
34. [34]
  Ackermann, L. Angew. Chem., Int. Ed, .2011, 50, 3842. doi: 10.1002/anie.201007883
35. [35]
  Huang, K.; Sun, C.-L.; Shi, Z.-J. Chem. Soc. Rev. 2011, 40, 2435. doi: 10.1039/c0cs00129e
36. [36]
  Börjesson, M.; Moragas, T.; Gallego, D.; Martin, R. ACS Catal. 2016, 6, 6739. doi: 10.1021/acscatal.6b02124
37. [37]
  Chen, Y.-G.; Xu, X.-T.; Zhang, K.; Li, Y.-Q.; Zhang, L.-P.; Fang, P.; Mei, T.-S. Synthesis 2018, 50, 35. doi: 10.1055/s-0036-1590908
38. [38]
  Riduan, S.-N.; Zhang, Y.; Ying, J.-Y. Angew. Chem., Int. Ed. 2009, 48, 3322. doi: 10.1002/anie.200806058
39. [39]
  Gomes, C.-D.-N.; Jacquet, O.; Villiers, C.; Thuery, P.; Ephritikhine, M.; Cantat, T. Angew. Chem., Int. Ed. 2012, 51, 187. doi: 10.1002/anie.201105516
40. [40]
  Xin, Z.; Lescot, C.; Friis, S. D.; Daasbjerg, K.; Skrydstrup, T. Angew. Chem., Int. Ed. 2015, 54, 6862. doi: 10.1002/anie.201500233
41. [41]
  Kielland, N.; Whiteoak, C.-J.; Kleij, A.-W. Adv. Synth. Catal. 2013, 355, 2115. doi: 10.1002/adsc.201300422
42. [42]
  Lu, X.-B.; Darensbourg, D.-J. Chem. Soc. Rev. 2012, 41, 1462. doi: 10.1039/C1CS15142H
43. [43]
  Decortes, A.; Castilla, A.-M.; Kleij, A.-W. Angew. Chem., Int. Ed. 2010, 49, 9822. doi: 10.1002/anie.201002087
44. [44]
  Vaitla, J.; Guttormsen, Y.; Mannisto, J.-K.; Nova, A.; Repo, T.; Bayer A.; Hopmann, K.-H. ACS Catal. 2017, 7, 7231. doi: 10.1021/acscatal.7b02306
45. [45]
  Sato, F.; Iijima, S.; Sato, M. J. Chem. Soc., Chem. Commun. 1981, 180.
46. [46]
  Beng, T.-K.; Gawley, R.-E. J. Am. Chem. Soc. 2010, 132, 12216. doi: 10.1021/ja105772z
47. [47]
  Perrona, Q.; Alexakis, A. Adv. Synth. Catal. 2010, 352, 2611. doi: 10.1002/adsc.201000517
48. [48]
  Egami, H.; Sato, K.; Asada, J.; Kawato, Y.; Hamashima, Y.; Tetrahedron 2015, 71, 6384. doi: 10.1016/j.tet.2015.05.041
49. [49]
  Takimoto, M.; Mori, M. J. Am. Chem. Soc. 2002, 124, 10008 doi: 10.1021/ja026620c
50. [50]
  Takimoto, M.; Nakamura, Y.; Kimura, K.; Mori, M. J. Am. Chem. Soc. 2004, 126, 5956. doi: 10.1021/ja049506y
51. [51]
  Ishii, M.; Mori, F.; Tanaka, K. Chem.-Eur. J. 2014, 20, 2169. doi: 10.1002/chem.201304623
52. [52]
  Williams, C.-M.; Johnson, J.-B.; Rovis, T. J. Am. Chem. Soc. 2008, 130, 14936. doi: 10.1021/ja8062925
53. [53]
  Greenhalgh, M.-D.; Thomas, S. P. J. Am. Chem. Soc. 2012, 134, 11900. doi: 10.1021/ja3045053
54. [54]
  Hayashi, C.; Hayashi, T.; Kikuchi, S.; Yamada, T. Chem. Lett. 2014, 43, 565. doi: 10.1246/cl.131163
55. [55]
  Hayashi, C.; Hayashi, T.; Yamada, T. Bull. Chem. Soc. Jpn. 2015, 88, 862. doi: 10.1246/bcsj.20150043
56. [56]
  Kawashima, S.; Aikawa, K.; Mikami, K.; Eur. J. Org. Chem. 2016, 19, 3166.
57. [57]
  Dian, L.; Müller, D.-S.; Marek, I. Angew. Chem., Int. Ed. 2017, 56, 6783. doi: 10.1002/anie.201701094
58. [58]
  Gui, Y.-Y.; Hu, N.; Chen, X.-W.; Liao, L.-L.; Ju, T.; Ye, J.-H.; Zhang, Z.; Li, J.; Yu, D.-G. J. Am. Chem. Soc. 2017, 139, 17011. doi: 10.1021/jacs.7b10149
59. [59]
  Chen, X.-W.; Zhu, L.; Gui, Y.-Y.; Jing, K.; Jiang, Y.-X.; Bo, Z.-Y.; Lan, Y.; Li J.; Yu, D.-G. J. Am. Chem. Soc. 2019, 141, 18825. doi: 10.1021/jacs.9b09721
60. [60]
  Qiu, J.; Gao, S.; Li, C.; Zhang, L.; Wang, Z.; Wang, X.; Ding, K.-L. Chem.-Eur. J. 2019, 25, 13874. doi: 10.1002/chem.201903906
61. [61]
  Feroci, M.; Orsini, M.; Palombi, L.; Sotgiu, G.; Colapietro, M.; Inesi, A. J. Org. Chem. 2004, 69, 487. doi: 10.1021/jo0343836
62. [62]
  Orsini, M.; Feroci, M.; Sotgiuand. G.; Inesi, A. Org. Biomol. Chem. 2005, 3, 1202. doi: 10.1039/b500570a
63. [63]
  Zhang, K.; Wang, H.; Zhao, S.-F.; Niu D.-F.; Lu, J.-X. J. Electroanal. Chem. 2009, 630, 35. doi: 10.1016/j.jelechem.2009.02.013
64. [64]
  Chen, B.-L.; Tu, Z.-Y.; Zhu, H.-W.; Sun, W.-W.; Wang, H.; Lu, J.-X. Electrochim. Acta 2014, 116, 475. doi: 10.1016/j.electacta.2013.11.001
65. [65]
  He, Q.; O'Brien, J.-W.; Kitselman, K.-A.; Tompkins, L.-E.; Curtis G.-C.-T.; Kerton, F.-M. Catal. Sci. Technol. 2014, 4, 1513. doi: 10.1039/C3CY00998J
66. [66]
  Sakakura, T.; Kohnoa, K. Chem. Commun. 2009, 45, 1312.
67. [67]
  Chen, B.-L.; Zhu, H.-W.; Xiao, Y.; Sun, Q.-L.; Wang, H.; Lu, J.-X. Electrochem. Commun. 2014, 42, 55. doi: 10.1016/j.elecom.2014.02.009
68. [68]
  Yang, H.-P.; Yue, Y.-N.; Sun, Q.-L.; Feng, Q.; Wang, H.; Lu, J.-X. Chem. Commun. 2015, 51, 12216. doi: 10.1039/C5CC04554A
69. [69]
  Jiao, K.-J.; Li, Z.-M.; Xu, X.-T.; Zhang, L.-P.; Li, Y.; Zhang, K.; Mei, T.-S. Org. Chem. Front. 2018, 5, 2244. doi: 10.1039/C8QO00507A
70. [70]
  Song, Q.-W.; Liu, P.; Han, L.-H.; Zhang K.; He, L.-N. Chin. J. Chem. 2018, 36, 147. doi: 10.1002/cjoc.201700572
71. [71]
  Niu, D.-F.; Xiao, L.-P.; Zhang, A.-J.; Zhang, G.-R.; Tan, Q.-Y.; Lu, J.-X. Tetrahedron 2008, 64, 10517. doi: 10.1016/j.tet.2008.08.093
72. [72]
  Isse, A.; Gennaro, A.; Vianello, E. J. Chem. Soc., Dalton Trans. 1996, 1613.
73. [73]
  Takeichi, T.; Ozaki, Y.; Takayama, Y. Chem. Lett. 1987, 1137.
74. [74]
  Yoshida, M.; Fujita, M.; Ishii, T.; Ihara, M. J. Am. Chem. Soc. 2003, 125, 4874. doi: 10.1021/ja0340681
75. [75]
  Yoshida, S.; Fukui, K.; Kikuchi, S.; Yamada, T. J. Am. Chem. Soc. 2010, 132, 4072. doi: 10.1021/ja1007118
76. [76]
  Yamada, W.; Sugawara, Y.; Cheng, H.-M. Ikeno, T.; Yamada, T. Eur. J. Org. Chem. 2007, 2007, 2604. doi: 10.1002/ejoc.200700169
77. [77]
  Vara, B.-A.; Struble, T.-J.; Wang, W.; Dobish, M.-C.; Johnston, J.-N. J. Am. Chem. Soc. 2015, 137, 7302. doi: 10.1021/jacs.5b04425
78. [78]
  Yousefi, R.; Struble, T.-J.; Payne, J.-L.; Vishe, M.; Schley, N.-D.; Johnston, J.-N. J. Am. Chem. Soc. 2019, 141, 618. doi: 10.1021/jacs.8b11793
79. [79]
  Gao, X.-T.; Gan, C.-C.; Liu, S.-Y.; Zhou, F.; Wu, H.-H.; Zhou, J. ACS Catal. 2017, 7, 8588. doi: 10.1021/acscatal.7b03370
80. [80]
  Gao, X.-T.; Xie, S.-L.; Zhou, F.; Wu, H.-H.; Zhou, J. Chem. Commun. 2019, 55, 14303. doi: 10.1039/C9CC07671A
81. [81]
  Xie, S.; Gao, X.; Zhou, F.; Wu, H.; Zhou, J. Chin. Chem. Lett. 2020, 31, 324. doi: 10.1016/j.cclet.2019.05.060
82. [82]
  Hartwig, J.-F.; Pouy, M.-J. Top. Organomet. Chem. 2011, 34, 169.
83. [83]
  Liu, W.-B.; Xia, J.-B.; You, S.-L. Top. Organomet. Chem. 2012, 38, 155. doi: 10.1021/ja210923k
84. [84]
  Qu, J.; Helmchen, G. Acc. Chem. Res. 2017, 50, 2539. doi: 10.1021/acs.accounts.7b00300
85. [85]
  Zhang, X.; Liu, W.-B.; Cheng, Q.; You, S.-L. Organometallics 2016, 35, 2467. doi: 10.1021/acs.organomet.6b00339
86. [86]
  Zhuo, C.-X.; Zhang X.; You, S.-L. ACS Catal. 2016, 6, 5307. doi: 10.1021/acscatal.6b01585
87. [87]
  Ye, K.-Y.; He, H.; Liu, W.-B.; Dai, L.-X.; Helmchen, G.; You, S.-L. J. Am. Chem. Soc. 2011, 133, 19006. doi: 10.1021/ja2092954
88. [88]
  Roggen, M.; Carreira, E.-M. J. Am. Chem. Soc. 2010, 132, 11917. doi: 10.1021/ja105271z
89. [89]
  Xia, J.-B.; Liu, W.-B.; Wang, T.-M.; You, S.-L. Chem.-Eur. J. 2010, 16, 6442. doi: 10.1002/chem.201000467
90. [90]
  Yamashita, Y.; Gopalarathnam, A; Hartwig, J.-F. J. Am. Chem. Soc. 2007, 129, 7508. doi: 10.1021/ja0730718
91. [91]
  Nemoto, T.; Sakamoto, T.; Matsumoto T.; Hamada, Y. Tetrahedron Lett. 2006, 47, 8737. doi: 10.1016/j.tetlet.2006.10.003
92. [92]
  Welter, C.; Moreno, R.-M.; Streiff, S.; Helmchen, G. Org. Biomol. Chem. 2005, 3, 3266. doi: 10.1039/b508634e
93. [93]
  Zheng, S.-C.; Zhang, M.; Zhao, X.-M. Chem.-Eur. J. 2014, 20, 7216. doi: 10.1002/chem.201402388
94. [94]
  Zhang, M.; Zhao X.; Zheng, S. Chem. Commun. 2014, 50, 4455. doi: 10.1039/c4cc00413b
95. [95]
  Liu, W.-B.; He, H.; Dai, L.-X.; You, S.-L. Synthesis 2009, 2076.
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4. [4]
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16. [16]
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17. [17]
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18. [18]
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Recent Advances of CO2 Fixation via Asymmetric Catalysis for the Direct Synthesis of Optically Active Small Molecules

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Recent Advances of CO₂ Fixation via Asymmetric Catalysis for the Direct Synthesis of Optically Active Small Molecules