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Selective Trifluoromethiolation and Difluoromethiolation of Pyridines at C(3) Position

  • Feng Chen ,
  • Fengling Qing
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  • CAS Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032
* Corresponding author. E-mail:

Online published: 2022-11-02

Cite this article

Feng Chen , Fengling Qing . Selective Trifluoromethiolation and Difluoromethiolation of Pyridines at C(3) Position[J]. Chinese Journal of Organic Chemistry, 2022 , 42(10) : 3423 -3424 . DOI: 10.6023/cjoc202200055

References

[1]
Meanwell, N. A. J. Med. Chem. 2018, 61, 5822.
[2]
Barata-Vallejo, S.; Bonesi, S.; Postigo, A. Org. Biomol. Chem. 2016, 14, 7150.
[3]
Zafrani, Y.; Yeffet, D.; Sod-Moriah, G.; Berliner, A.; Amir, D.; Marciano, D.; Gershonov, E.; Saphier, S. J. Med. Chem. 2017, 60, 797.
[4]
(a) Nagib, D. A.; MacMillan, D. W. Nature 2011, 480, 224.
[4]
(b) Ji, Y.; Brueckl, T.; Baxter, R. D.; Fujiwara, Y.; Seiple, I. B.; Su, S.; Blackmond, D. G.; Baran, P. S. Proc. Natl. Acad. Sci. U. S. A. 2011, 108, 14411.
[4]
(c) Yang, B.; Yu, D.; Xu, X.-H.; Qing, F.-L. ACS Catal. 2018, 8, 2839.
[4]
(d) Zhang, X.; Nottingham, K. G.; Patel, C.; Alegre-Requena, J. V.; Levy, J. N.; Paton, R. S.; McNally, A. Nature 2021, 594, 217.
[5]
(a) Wu, J.; Shen, Q. Acc. Chem. Res. 2021, 54, 2946.
[5]
(b) Shao, X.; Xu, C.; Lu, L.; Shen, Q. Acc. Chem. Res. 2015, 48, 1227.
[6]
Murakami, K.; Orcid, S. Y.; Kaneda, T.; Itami, K. Chem. Rev. 2017, 117, 9302.
[7]
Liu, Z.; He, J.-H.; Zhang, M.; Shi, Z.-J.; Tang, H.; Zhou, X.-Y.; Tian, J.-J.; Wang, X.-C. J. Am. Chem. Soc. 2022, 144, 4810.
[8]
Zhou, X.-Y.; Zhang, M.; Liu, Z.; He, J.-H.; Wang, X.-C. J. Am. Chem. Soc. 2022, 144, 14463.
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