Citation: Kong Yaolei, Sun Xiaotong, Weng Jianquan. Selectfluor as "Fluorine-Free" Functional Reagent Applied to Organic Synthesis under Transition Metal-Free Conditions[J]. Chinese Journal of Organic Chemistry, ;2020, 40(9): 2641-2657. doi: 10.6023/cjoc202004005 shu

Selectfluor as "Fluorine-Free" Functional Reagent Applied to Organic Synthesis under Transition Metal-Free Conditions

College of Chemical Engineering, Zhejiang University of Technology, Hangzhou 310014

Corresponding author: Weng Jianquan, jqweng@zjut.edu.cn
Received Date: 2 April 2020
Revised Date: 13 May 2020
Available Online: 11 June 2020
Fund Project: Project supported by the Natural Science Foundation of Zhejiang Province (No. LY17C140003)the Natural Science Foundation of Zhejiang Province LY17C140003

Figures(28)

Selectfluor, a commercial electrophilic fluorination reagent with superior performance, is widely used in fluorination reactions. In recent years, Selectfluor has also been widely applied as "fluorine-free" functional reagent in organic synthesis. Especially the application of Selectfluor/transition metals synergetic catalytic system has made great progress. However, this catalytic system has some disadvantages, such as the use of expensive transition metals and environmental unfriendliness. Therefore, more and more attention has been paid to the application of Selectfluor as "fluorine-free" functional reagent under transition metal-free conditions. In this paper, classified by the type of reactions, the research progress of Selectfluor as a "fluorine-free" functional reagent in organic synthesis under transition metal-free conditions is reviewed, and their future outlook is also discussed.
- Selectfluor,
- "fluorine-free" functional reagent,
- transition metal-free,
- organic synthesis
1. [1]
  Singh, R. P.; Shreeve, J. M. Acc. Chem. Res. 2004, 37, 31. doi: 10.1021/ar030043v
2. [2]
  Campbell, M. G.; Ritter, T. Chem. Rev. 2015, 115, 612. doi: 10.1021/cr500366b
3. [3]
  Champagne, P. A.; Desroches, J.; Hamel, J. D.; Vandamme, M.; Paquin, J. F. Chem. Rev. 2015, 115, 9073. doi: 10.1021/cr500706a
4. [4]
  Huang, Y.-L.; Chen, Q. Chin. J. Org. Chem. 2017, 37, 2745 (in Chinese).
5. [5]
  Tian, Y.; Zhou, G.; Zhao, X.; Dan, W. Acta Chim. Sinica 2018, 76, 962 (in Chinese).
6. [6]
  Hu, J.; Yang, Y.; Lou, Z.; Ni, C.; Hu, J. Chin. J. Chem. 2018, 36, 1202. doi: 10.1002/cjoc.201800426
7. [7]
  Kandula, V.; Thota, P. K.; Mallesham, P.; Raghavulu, K.; Chatterjee, A.; Yennam, S.; Behera, M. Synlett 2019, 30, 2295. doi: 10.1055/s-0039-1691489
8. [8]
  Fuchigami, T.; Inagi, S. Acc. Chem. Res. 2020, 53, 322. doi: 10.1021/acs.accounts.9b00520
9. [9]
  Stavber, S. Molecules 2011, 16, 6432. doi: 10.3390/molecules16086432
10. [10]
  Yang, K.; Song, M.-J.; Ali, A. I. M.; Mudassir, S. M.; Ge, H.-B. Chem. Asian J. 2020, 15, 729. doi: 10.1002/asia.202000011
11. [11]
  Brand, J. P.; Li, Y.; Waser, J. Isr. J. Chem. 2013, 53, 901. doi: 10.1002/ijch.201300044
12. [12]
  Miro, J.; Del Pozo, C. Chem. Rev. 2016, 116, 11924. doi: 10.1021/acs.chemrev.6b00203
13. [13]
  Zhu, S.-F.; Chen, K. Synlett 2017, 28, 640. doi: 10.1055/s-0036-1588693
14. [14]
  Xu, Q.; Gu, P.; Wang, F.-J.; Shi, M. Org. Chem. Front. 2015, 2, 1475. doi: 10.1039/C5QO00155B
15. [15]
  Liu, J.-B.; Xu, X.-H.; Qing, F.-L. Org. Lett. 2015, 17, 5048. doi: 10.1021/acs.orglett.5b02522
16. [16]
  Fu, M.-L.; Liu, J.-B.; Xu, X.-H.; Qing, F.-L. J. Org. Chem. 2017, 82, 3702. doi: 10.1021/acs.joc.7b00190
17. [17]
  Zhang, J.; Wang, H.; Ren, S.-B.; Zhang, W.-X.; Liu, Y.-K. Chin. J. Org. Chem. 2015, 35, 2650 (in Chinese).
18. [18]
  Zheng, L.-M.; Shi, D.-D.; Bao, H.-Y.; Liu, Y.-K. Chin. J. Org. Chem. 2019, 39, 2821 (in Chinese).
19. [19]
  Shi, D.-D.; Bao, H.-Y.; Xu, Z.; Liu, Y.-K. Chin. J. Org. Chem. 2017, 37, 1290 (in Chinese).
20. [20]
  Samanta, S.; Hajra, A. J. Org. Chem. 2019, 84, 4363. doi: 10.1021/acs.joc.9b00366
21. [21]
  Kumaraswamy, G.; Gangadhar, M.; Ramesh, V.; Ankamma, K.; Sridhar, B. Org. Lett. 2019, 21, 6300. doi: 10.1021/acs.orglett.9b02180
22. [22]
  Daniels, M. H.; Hubbs, J. Tetrahedron Lett. 2011, 52, 3543. doi: 10.1016/j.tetlet.2011.05.012
23. [23]
  Liu, L.; Wang, J.-B.; Zhou, H.-W. J. Org. Chem. 2015, 80, 4749. doi: 10.1021/acs.joc.5b00261
24. [24]
  Liang, X.-A.; Niu, L.-B.; Wang, S.-C.; Liu, J.-M.; Lei, A. Org. Lett. 2019, 21, 2441. doi: 10.1021/acs.orglett.9b00744
25. [25]
  Niu, L.-B.; Liu, J.-M.; Liang, X.-A.; Wang, S.-C.; Lei, A. Nat. Commun. 2019, 10, 467. doi: 10.1038/s41467-019-08413-9
26. [26]
  Zhao, H.; Jin, J. Org. Lett. 2019, 21, 6179. doi: 10.1021/acs.orglett.9b01635
27. [27]
  Galloway, J. D.; Baxter, R. D. Tetrahedron 2019, 75, 130665. doi: 10.1016/j.tet.2019.130665
28. [28]
  Shi, D.; Qin, H.-T.; Zhu, C.; Liu, F. Eur. J. Org. Chem. 2015, 2015, 5084. doi: 10.1002/ejoc.201500780
29. [29]
  Lv, Y.-H.; Sun, K.; Pu, W.-Y.; Mao, S.-K.; Li, G.; Niu, J.-J.; Chen, Q.; Wang, T.-T. RSC Adv. 2016, 6, 93486. doi: 10.1039/C6RA22653A
30. [30]
  Sun, B.; Yin, S.; Zhuang, X.-H.; Jin, C.; Su, W.-K. Org. Biomol. Chem. 2018, 16, 6017. doi: 10.1039/C8OB01348A
31. [31]
  Yuan, J.-W.; Zeng, F.-L.; Mai, W.-P.; Yang, L.-R.; Xiao, Y.-M.; Mao, P.; Wei, D.-H. Org. Biomol. Chem. 2019, 17, 5038. doi: 10.1039/C9OB00509A
32. [32]
  Yang, Z.; Chen, S.-W.; Yang, F.; Zhang, C.-X.; Dou, Y.; Zhou, Q.-J.; Yan, Y.-Z.; Tang, L. Eur. J. Org. Chem. 2019, 5998.
33. [33]
  Tang, L.; Yang, Z.; Yang, F.; Huang, Y.-F.; Chen, H.-F.; Cheng, H.; Song, W.-Y.; Ren, B.; Zhou, Q.-J. ChemistrySelect 2019, 4, 12053. doi: 10.1002/slct.201903856
34. [34]
  Yadav, J. S.; Reddy, B. V. S.; Reddy, Y. J. Tetrahedron Lett. 2007, 48, 7034. doi: 10.1016/j.tetlet.2007.07.130
35. [35]
  Yadav, J. S.; Reddy, B. V. S.; Reddy, Y. J. Chem. Lett. 2008, 37, 652. doi: 10.1246/cl.2008.652
36. [36]
  Abonia, R.; Gutierrez, L. F.; Zwarycz, A. T.; Correa Smits, S.; Laali, K. K. Heteroat. Chem. 2019, 2019, 1.
37. [37]
  Wu, D.-Z.; Yang, X.-J.; Wu, L.-Q. J. Chem. Sci. 2012, 124, 901. doi: 10.1007/s12039-012-0270-0
38. [38]
  Khazaei, A.; Rahmati, S.; Khalafi-nezhad, A.; Saednia, S. J. Fluorine Chem. 2012, 137, 123. doi: 10.1016/j.jfluchem.2012.03.005
39. [39]
  Chen, Y.; Qi, H.-Y.; Chen, N.; Ren, D.-M.; Xu, J.-X.; Yang, Z.-H. J. Org. Chem. 2019, 84, 9044. doi: 10.1021/acs.joc.9b00965
40. [40]
  Li, X.-F.; Fu, X.-L.; Huang, Y.-L.; Yan, Z.-Y. J. Chem. Res. 2018, 202.
41. [41]
  Huang, Y.-L.; Lei, J.-Y.; Fu, X.-L.; Xie, W.-L.; Li, X.-F. J. Chem. Res. 2019, 43, 179. doi: 10.1177/1747519819857478
42. [42]
  Xie, L.-Y.; Qu, J.; Peng, S.; Liu, K.-J.; Wang, Z.; Ding, M.-H.; Wang, Y.; Cao, Z.; He, W.-M. Green Chem. 2018, 20, 760. doi: 10.1039/C7GC03106H
43. [43]
  Yuan, J.-W.; Zhu, J.-L.; Li, B.; Yang, L.-Y.; Mao, P.; Zhang, S.-R.; Li, Y.-C.; Qu, L.-B. Org. Biomol. Chem. 2019, 17, 10178. doi: 10.1039/C9OB02157D
44. [44]
  Chen, Q.; Zeng, J.-K.; Yan, X.-X.; Huang, Y.-L.; Wen, C.-X.; Liu, X.-G.; Zhang, K. J. Org. Chem. 2016, 81, 10043. doi: 10.1021/acs.joc.6b01932
45. [45]
  Yang, K.; Zhang, H.; Niu, B.; Tang, T.-D.; Ge, H.-B. Eur. J. Org. Chem. 2018, 2018, 5520. doi: 10.1002/ejoc.201801090
46. [46]
  Mai, W.-P.; Yuan, J.-W.; Zhu, J.-L.; Li, Q.-Q.; Yang, L.-R.; Xiao, Y.-M.; Mao, P.; Qu, L.-B. ChemistrySelect 2019, 4, 11066. doi: 10.1002/slct.201903478
47. [47]
  Zupan, M.; Iskra, J.; Stavber, S. Tetrahedron Lett. 1997, 38, 6305. doi: 10.1016/S0040-4039(97)01414-7
48. [48]
  Chiappe, C.; Pieraccini, D. ARKIVOC 2002, 249.
49. [49]
  Stavber, S.; Jereb, M.; Zupan, M. Chem. Commun. 2002, 488.
50. [50]
  Jereb, M.; Stavber, S.; Zupan, M. Tetrahedron 2003, 59, 5935. doi: 10.1016/S0040-4020(03)00904-9
51. [51]
  Ye, C.-F.; Shreeve, J. M. J. Org. Chem. 2004, 69, 8561. doi: 10.1021/jo048383x
52. [52]
  Pavlinac, J.; Zupan, M.; Stavber, S. J. Org. Chem. 2006, 71, 1027. doi: 10.1021/jo052021n
53. [53]
  Krow, G. R.; Gandla, D.; Guo, W. W.; Centafont, R. A.; Lin, G. L.; DeBrosse, C.; Sonnet, P. E.; Ross, C. W.; Ramjit, H. G.; Cannon, K. C. J. Org. Chem. 2008, 73, 2122. doi: 10.1021/jo702155v
54. [54]
  Khupse, R. S.; Erhardt, P. W. Org. Lett. 2008, 10, 5007. doi: 10.1021/ol802112r
55. [55]
  Mal, D.; De, S. R. Org. Lett. 2009, 11, 4398. doi: 10.1021/ol901817r
56. [56]
  Laali, K. K.; Nandi, G. C.; Bunge, S. D. Tetrahedron Lett. 2014, 55, 2401. doi: 10.1016/j.tetlet.2014.02.110
57. [57]
  Shi, L.-L.; Zhang, D.-M.; Lin, R.-Y.; Zhang, C.; Li, X.; Jiao, N. Tetrahedron Lett. 2014, 55, 2243. doi: 10.1016/j.tetlet.2014.02.071
58. [58]
  Dannenberg, C. A.; Bizet, V.; Zou, L.-H.; Bolm, C. Eur. J. Org. Chem. 2015, 2015, 77. doi: 10.1002/ejoc.201403352
59. [59]
  Liang, D.-Q.; Li, X.-G.; Wang, C.-W.; Dong, Q.-S.; Wang, B.-L.; Wang, H. Tetrahedron Lett. 2016, 57, 5390. doi: 10.1016/j.tetlet.2016.10.092
60. [60]
  Huang, B.-B.; Zhao, Y.-T.; Yang, C.; Gao, Y.; Xia, W.-J. Org. Lett. 2017, 19, 3799. doi: 10.1021/acs.orglett.7b01427
61. [61]
  Qi, H.; Li, X.; Liu, Z.; Miao, S.-S.; Fang, Z.; Chen, L.; Fang, Z.; Guo, K. ChemistrySelect 2018, 3, 10689. doi: 10.1002/slct.201802925
62. [62]
  Scheidt, F.; Neufeld, J.; Schafer, M.; Thiehoff, C.; Gilmour, R. Org. Lett. 2018, 20, 8073. doi: 10.1021/acs.orglett.8b03794
63. [63]
  Sarie, J. C.; Neufeld, J.; Daniliuc, C. G.; Gilmour, R. ACS Catal. 2019, 9, 7232. doi: 10.1021/acscatal.9b02313
64. [64]
  Hu, J.; Zhou, G.; Tian, Y.-W.; Zhao, X.-M. Org. Biomol. Chem. 2019, 17, 6342. doi: 10.1039/C9OB00972H
65. [65]
  Blank, S. J.; Stephens, C. E. Tetrahedron Lett. 2006, 47, 6849. doi: 10.1016/j.tetlet.2006.07.071
66. [66]
  Kirihara, M.; Naito, S.; Ishizuka, Y.; Hanai, H.; Noguchi, T. Tetrahedron Lett. 2011, 52, 3086. doi: 10.1016/j.tetlet.2011.03.132
67. [67]
  Wu, D.-G.; Zhang, J.; Wang, H.; Zhang, J.-H.; Liu, Y.-K.; Liu, M.-C. Asian J. Org. Chem. 2014, 3, 1163. doi: 10.1002/ajoc.201402171
68. [68]
  Wang, H.; Ren, S.-B.; Zhang, J.; Zhang, W.; Liu, Y.-K. J. Org. Chem. 2015, 80, 6856. doi: 10.1021/acs.joc.5b00857
69. [69]
  Rajawinslin, R. R.; Raihan, M. J.; Janreddy, D.; Kavala, V.; Kuo, C.-W.; Kuo, T.-S.; Chen, M.-L.; He, C.-H.; Yao, C.-F. Tetrahedron 2014, 70, 7505. doi: 10.1016/j.tet.2014.08.024
70. [70]
  Lv, Y.-H.; Wang, X.; Cui, H.; Sun, K.; Pu, W.-Y.; Li, G.; Wu, Y.-T.; He, J.-L.; Ren, X.-R. RSC Adv. 2016, 6, 74917. doi: 10.1039/C6RA16266E
71. [71]
  Allmann, T. C.; Moldovan, R. P.; Jones, P. G.; Lindel, T. Chem. Eur. J. 2016, 22, 111. doi: 10.1002/chem.201503695
72. [72]
  Chen, Q.; Zeng, J.-K.; Yan, X.-X, ; Huang, Y.-L.; Du, Z.-Y.; Zhang, K.; Wen, C.-X. Tetrahedron Lett. 2016, 57, 3379. doi: 10.1016/j.tetlet.2016.06.078
73. [73]
  Bohlmann, R.; Hauser, A. Synlett 2016, 27, 1870. doi: 10.1055/s-0035-1561642
74. [74]
  Jiang, X.-J.; Yang, J.-J.; Zhang, F.; Yu, P.; Yi, P.; Sun, Y.-W.; Wang, Y.-Q. Org. Lett. 2016, 18, 3154. doi: 10.1021/acs.orglett.6b01367
75. [75]
  Xie, L.-Y.; Peng, S.; Liu, F.; Yi, J.-Y.; Wang, M.; Tang, Z.; Xu, X.; He, W.-M. Adv. Synth. Catal. 2018, 360, 4259. doi: 10.1002/adsc.201800918
76. [76]
  Shah, S. T. A.; Singh, S.; Guiry, P. J. J. Org. Chem. 2009, 74, 2179. doi: 10.1021/jo802494t
77. [77]
  Xie, L.-J.; Wang, R.-L.; Wang, D.; Liu, L.; Cheng, L. Chem. Commun. 2017, 53, 10734. doi: 10.1039/C7CC05544G
78. [78]
  Wang, S.-C.; Liu, J.-M.; Niu, L.-B.; Yi, H.; Chiang, C.-W.; Lei, A. J. Photochem. Photobiol., A 2018, 355, 120. doi: 10.1016/j.jphotochem.2017.09.075
79. [79]
  Zeng, Y.-J.; Duan, Y.; Zhao, H.; Hu, X.-G. Chin. J. Org. Chem. 2018, 38, 1712 (in Chinese).
80. [80]
  Yadav, J. S.; Reddy, B. V. S.; Sunitha, V.; Reddy, K. S. Adv. Synth. Catal. 2003, 345, 1203. doi: 10.1002/adsc.200303101
81. [81]
  Kumar, B. S.; Reddy, Y. T.; Reddy, P. N.; Kumar, P. S.; Rajitha, B. J. Heterocyclic Chem. 2006, 43, 477. doi: 10.1002/jhet.5570430233
82. [82]
  Ranjbar-Karimi, R.; Hashemi-Uderji, S.; Mousavi, M. J. Iran. Chem. Soc. 2011, 8, 193. doi: 10.1007/BF03246215
83. [83]
  Heravi, M. R. P. J. Iran. Chem. Soc. 2009, 6, 483. doi: 10.1007/BF03246525
84. [84]
  Ye, W.-M.; Li, W.-B.; Zhang, J.-L. Chem. Commun. 2014, 50, 9879. doi: 10.1039/C4CC03450C
85. [85]
  Wei, D.-L.; Li, Y.-R.; Liang, F.-S. Adv. Synth. Catal. 2016, 358, 3887. doi: 10.1002/adsc.201600587
86. [86]
  Yan, D.-M.; Zhao, Q.-Q.; Rao, L.; Chen, J.-R.; Xiao, W.-J. Chem. Eur. J. 2018, 24, 16895. doi: 10.1002/chem.201804229
87. [87]
  Gao, Y.-J.; Hider, R. C.; Ma, Y.-M. RSC Adv. 2019, 9, 10340. doi: 10.1039/C9RA01481K
88. [88]
  Chen, J.; Ding, Y.-X.; Gao, Y.-J.; Zhou, D.-H.; Hider, R.; Ma, Y.-M. Chemistryselect 2019, 4, 2404. doi: 10.1002/slct.201900113
89. [89]
  He, G.-K.; Li, Y.; Yu, Z.-L.; Chen, Z.-Q.; Tang, Y.-M.; Song, G.-L.; Loh, T. P. Org. Chem. Front. 2019, 6, 3644. doi: 10.1039/C9QO00845D
90. [90]
  Wu, F.; Alom, N. E.; Ariyarathna, J. P.; Nass, J.; Li, W. Angew. Chem., Int. Ed. 2019, 58, 11676. doi: 10.1002/anie.201904662
91. [91]
  Liu, J.-J.; Wong, C.-H. Tetrahedron Lett. 2002, 43, 3915. doi: 10.1016/S0040-4039(02)00640-8
92. [92]
  Yadav, J. S.; Reddy, B. V. S.; Reddy, C. S. Tetrahedron Lett. 2004, 45, 1291. doi: 10.1016/j.tetlet.2003.11.102
93. [93]
  Shinu, V. S.; Sheeja, B.; Purushothaman, E.; Bahulayan, D. Tetrahedron Lett. 2009, 50, 4838. doi: 10.1016/j.tetlet.2009.06.022
94. [94]
  Sun, K.; Zhu, Z.-H.; Sun, J.-J.; Liu, L.-L.; Wang, X. J. Org. Chem. 2016, 81, 1476. doi: 10.1021/acs.joc.5b02593
95. [95]
  Muñiz, K.; Wöste, T. Synthesis 2016, 48, 816. doi: 10.1055/s-0035-1561313
96. [96]
  Rezayati, S.; Hajinasiri, R.; Erfani, Z. Res. Chem. Intermed. 2016, 42, 2567. doi: 10.1007/s11164-015-2168-1
97. [97]
  Yan, M.; Zhou, D.-H.; Gao, Y.-J.; Ma, Y.-M. ChemistrySelect 2018, 3, 13006. doi: 10.1002/slct.201802450
98. [98]
  Cao, Y.; Zhou, D.-H.; Ma, Y.-M. Can. J. Chem. 2019, 97, 37. doi: 10.1139/cjc-2018-0181
99. [99]
  Gao, Y.-J.; Zhou, D.-H.; Ma, Y.-M. ChemistrySelect 2018, 3, 9374. doi: 10.1002/slct.201801996
100. [100]
  Sharma, P.; Sharma, R. K. Chirality 2019, 31, 91. doi: 10.1002/chir.23039
101. [101]
  Yang, K.; Li, Y.; Ma, Z.-Y.; Tang, L.; Yin, Y.; Zhang, H.; Li, Z.-Y.; Sun, X.-Q. Eur. J. Org. Chem. 2019, 2019, 5812. doi: 10.1002/ejoc.201900960
102. [102]
  Bao, H.-Y.; Hu, X.-J.; Zhang, J.; Liu, Y.-K. Tetrahedron 2019, 75, 130533. doi: 10.1016/j.tet.2019.130533
103. [103]
  Yang, K.; Niu, B.; Ma, Z.-Y.; Wang, H.; Lawrence, B.; Ge, H.-B. J. Org. Chem. 2019, 84, 14045. doi: 10.1021/acs.joc.9b02202
104. [104]
  Xu, W.-X.; Dai, X.-Q.; Xu, H.-J.; Weng, J.-Q. Chin. J. Org. Chem. 2018, 38, 2807 (in Chinese).
105. [105]
  Kong, Y.-L.; Xu, W.-X.; Ye, F.-X.; Weng, J.-Q. Chin. J. Org. Chem. 2019, 39, 3065 (in Chinese).
106. [106]
  Tréguier, B.; Roche, S. P. Org. Lett. 2014, 16, 278. doi: 10.1021/ol403281t
107. [107]
  Liang, D.-Q.; Li, X.-G.; Lan, Q.; Huang, W.-Z.; Yuan, L.; Ma, Y.-H. Tetrahedron Lett. 2016, 57, 2207. doi: 10.1016/j.tetlet.2016.04.028
108. [108]
  Liang, D.-Q.; Li, Y.-N.; Gao, S.-L.; Li, R.-L.; Li, X.-G.; Wang, B.-L.; Yang, H. Green Chem. 2017, 19, 3344. doi: 10.1039/C7GC00356K
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13. [13]
  . Synthesis and properties of metal‐organic frameworks. Chinese Journal of Inorganic Chemistry, 2025, 41(10): 1-2.
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15. [15]
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沈阳化工大学材料科学与工程学院沈阳 110142