Direct construction of sulfenylated pyrazoles catalyzed by I2 at room temperature

doi:10.1016/S1872-2067(17)62901-2

Abstract

ShuangHong Hao, LiXia Li, DaoQing Dong, ZuLi Wang. Direct construction of sulfenylated pyrazoles catalyzed by I₂ at room temperature[J]. Chinese Journal of Catalysis, 2017, 38(10): 1664-1667.

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[1] E. Block, Reactions of Organosulfur Compounds, Academic Press, New York, 1978.
[2] A. Gangjee, Y. B. Zeng, T. Talreja, J. J. Mc Guire, R. L. Kisliuk, S. F. Queener, J. Med. Chem., 2007, 50, 3046-3053.
[3] S. Patai, Z. Rappoport, The Chemistry of Organic Selenium and Tellurium Compounds, Wiley, New York, 1987, Vols. 1-2.
[4] N. V. Zyk, E. K. Beloglazkina, M. A. Belova, N. S. Dubinina, Russ. Chem. Rev., 2003, 72, 769-786.
[5] M. D. McReynolds, J. M. Dougherty, P. R. Hanson, Chem. Rev., 2004, 104, 2239-2258.
[6] W. Huang, G. F. Yang, Bioorg. Med. Chem., 2006, 14, 8280-8285.
[7] D. Dang, Z. Wang, W. Q. Lin, W. L. Song, Chin. J. Catal., 2016, 37, 720-726.
[8] N. Nowrouzi, M. Abbasi, H. Latifi, Chin. J. Catal., 2016, 37, 1550-1554.
[9] Z. J. Chen, J. Y. Chen, Y. W. Li, Chin. J. Catal., 2017, 38, 1108-1126.
[10] S. K. Pulakhandam, N. K. Katari, R. P. Manda, J. Chem. Sci., 2017, 129, 203-210.
[11] A. N. Desnoyer, J. A. Love, Chem. Soc. Rev., 2017, 46, 197-238.
[12] C. F. Lee, Y. C. Liu, S. S. Badsara, Chem. Asian J., 2014, 9, 706-722.
[13] C. Shen, P. F. Zhang, Q. Sun, S. Q. Bai, T. S. A. Hor, X. G. Liu, Chem. Soc. Rev., 2015, 44, 291-314.
[14] S. I. Fukuzawa, E. Shimizu, Y. Atsuumi, M. Haga, K. Ogata, Tetrohedron Lett., 2009, 50, 2374-2376.
[15] W. J. Wang, X. C. Wang, Heterocycles, 2017, 94, 449-464.
[16] K. J. Wei, Z. J. Quan, Z. Zhang, Y. X. Da, X. C. Wang, RSC Adv., 2016, 6, 78059-78063.
[17] K. J. Wei, Z. J. Quan, Z. Zhang, Y. X. Da, X. C. Wang, Org. Biomol. Chem., 2016, 14, 2395-2398.
[18] B. X. Du, Z. J. Quan, Y. X. Da, Z. Zhang, X. C. Wang, Adv. Synth. Catal., 2015, 357, 1270-1276.
[19] D. S. Yang, P. F. Sun, W. Wei, L. D. Meng, L. C. He, B. K. Fang, W. Jiang, H. Wang, Org. Chem. Front., 2016, 3, 1457-1461.
[20] D. S. Yang, K. L. Yan, W. Wei, J. Zhao, M. Q. Zhang, X. G. Sheng, G. Q. Li, S. L. Lu, H. Wang, J. Org. Chem., 2015, 80, 6083-6092.
[21] F. L. Yang, S. K. Tian, Angew. Chem. Int. Ed., 2013, 52, 4929-4932.
[22] T. Miao, P. H. Li, Y. C. Zhang, L. Wang, Org. Lett., 2015, 17, 832-835.
[23] Y. T. Dong, Q. Jin, L. Zhou, J. Chen, Org. Lett., 2016, 18, 5708-5711.
[24] L. Fang, A. J. Lin, Y. Shi, Y. X. Cheng, C. J. Zhu, Tetrahedron Lett., 2014, 55, 387-389.
[25] K. Liao, J. S. Yu, W. M. Gao, F. Zhou, J. Zhou, Chem. Commun., 2015, 51, 16255-16258.
[26] F. L. Yang, Y. Gui, B. K. Yu, Y. X. Jin, S. K. Tian, Adv. Synth. Catal., 2016, 358, 3368-3372.
[27] Y. Siddaraju, K. R. Prabhu, Org. Biomol. Chem., 2017, 15, 5191-5196.
[28] D. S. Yang, P. F. Sun, W. Wei, L. D. Meng, L. C. He, B. K. Fang, W. Jiang, H. Wang, Org. Chem. Front., 2016, 3, 1457-1461.
[29] Y. F. Liao, P. C. Jiang, S. P. Chen, H. R. Qi, G. J. Deng, Green Chem., 2013, 15, 3302-3306.
[30] K. L. Yan, D. S. Yang, P. F. Sun, W. Wei, Y. Liu, G. Q. Li, S. L. Lu, H. Wang, Tetrahedron Lett., 2015, 56, 4792-4795.
[31] P. F. Sun, D. S. Yang, W. Wei, X. J. Sun, W. H. Zhang, H. Zhang, Y. Wang, H. Wang, Tetrahedron, 2017, 73, 2022-2029.
[32] P. F. Sun, D. S. Yang, W. Wei, L. H. Jiang, Y. Q. Wang, T. X. Dai, H. Wang, Org. Chem. Front., 2017, 4, 1367-1371.
[33] Y. Siddaraju, K. R. Prabhu, J. Org. Chem., 2016, 81, 7838-7846.
[34] Z. C. Gao, X. Zhu, R. H. Zhang, RSC Adv. 2014, 4, 19891.
[35] X. Zhao, X. Y. Lu, A. Q. Wei, X. L. Jia, J. Chen, K. Lu, Tetrahedron Lett., 2016, 57, 5330-5333.
[36] J. P. Wan, S. S. Zhong, L. L. Xie, X. J. Cao, Y. Y. Liu, L. Wei, Org. Lett., 2016, 18, 584-587.
[37] D. S. Yang, K. L. Yan, W. Wei, J. Zhao, M. Q. Zhang, X. Q. Sheng, G. Q. Li, S. L. Lu, H. Wang, J. Org. Chem., 2015, 80, 6083-6092.
[38] X. Y. Qian, S. Q. Li, J. S. Song, H. C. Xu, ACS Catal., 2017, 7, 2730-2734.
[39] D. Q. Dong, H. Zhang, Z. L. Wang, RSC Adv., 2017, 7, 3780-3782.
[40] H. Zhang, D. Q. Dong, S. H. Hao, Z. L. Wang, RSC Adv., 2016, 6, 8465-8468.
[41] X. X. Liu, H. H. Cui, D. S. Yang, S. C. Dai, T. T. Zhang, J. Y. Sun, W. Wei, H. Wang, RSC Adv., 2016, 6, 51830-51833.
[45] C. Ravi, D. Chandra Mohan, S. Adimurthy, Org. Lett., 2014, 16, 2978-2981.
[43] W. L. Ge, Y. Y. Wei, Green Chem., 2012, 14, 2066-2070.
[44] N. Devi, R. Rahaman, K. Sarma, P. Barman, Eur. J. Org. Chem., 2016, 384-388.
[45] X. M. Ji, S. J. Zhou, F. Chen, X. Q. Zhang, R. Y. Tang, Synthesis, 2015, 47, 659-671.

Direct construction of sulfenylated pyrazoles catalyzed by I₂ at room temperature

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