Visible Light Photoredox-Induced Smiles Rearrangement
Received date: 2019-05-14
Online published: 2019-06-04
Supported by
Project supported by the National Natural Science Foundation of China(No.21772121);the “Thousand Plan” Youth program.
The intramolecular aromatic ring systems migration reactions, namely Smiles rearrangement is a powerful method for (hetero)aryl group functionalization. It can be employed as a complementary strategy to arene functionalization, and has found its broad applications in synthetic chemistry. After the initial documentation in 1894 this chemistry was intensively investigated by Smiles. In its classical pathway, the migration of aromatic ring system takes place ipso nucleophilic substitution. Accordingly, the migrating (hetero)aryl groups are highly electronic and steric-dependent. Moreover, as new reaction modes reported, advances have been made in the areas for arene C—C, C—N and C—O bond formation and radical triggered Smiles rearrangement has also enriched migrating units. Recently, there has been a rapid growth in the transformation induced by visible-light photocatalysis. Harnessing visible light as the energy source for chemical reactions usually serves as an environmentally benign alternative in comparison with classical radical pathway. Furthermore, photoredox-induced rearrangement represents a valuable and efficient approach for facilitating both the radical-based bond-cleaving and bond-forming events in a single step. It has become an effective tool for both synthesis and late stage modification of bio-active molecules. The last five years has witnessed many important advances in exploring photo-induced Smiles reactions, which make this classic reaction regained its attention. Significant progress has been made for expediting the generation of N-centered, C-centered and O-centered from a variety of precursors before single electron transfer rearrangement. This powerful synthetic platform for efficient promotes (hetero) aromatic group construction under mild reaction conditions, and has become a useful method for the synthesis and late stage functionalization of pharmaceutically interest products. In this perspective, we focus on visible light induced Smiles chemistry, which the major breakthroughs are classified based on migrating-induced radical species, and their synthetic applications are discussed briefly.
Yilin Chen, , Liang Chang, , Zhiwei Zuo, . Visible Light Photoredox-Induced Smiles Rearrangement[J]. Acta Chimica Sinica, 2019 , 77(9) : 794 -802 . DOI: 10.6023/A19050179
[1] | (a) Chen, Z.-M.; Zhang, X.-M.; Tu, Y.-Q. Chem. Soc. Rev. 2015, 44, 5220 |
[1] | (b) Allart-Simon, I.; Gérard, S.; Sapi, J. Molecules 2016, 21, 878; |
[1] | (c) Holden, C. M.; Greaney, M. F. Chem. Eur. J. 2017, 23, 8992; |
[1] | (d) Lin, S.-B.; He, X.-R.; Meng, J.-P.; Gu, H.-N.; Zhang, P.-Z.; Wu, J. Chin. J. Org. Chem. 2017, 37, 1864. |
[1] | ( 蔺松波, 何兴瑞, 孟金鹏, 顾海宁, 张培志, 吴军, 有机化学, 2017, 37, 1864.) |
[2] | (a) Warren, L. A.; Smiles, S. J. Chem. Soc. 1930, 1327 |
[2] | (b) Warren, L. A.; Smiles, S. J. Chem. Soc. 1930, 956; |
[2] | (c) Levi, A.; Warren, L. A.; Smiles, S. J. Chem. Soc. 1933, 1490. |
[3] | (a) Kong, W.; Merino, E.; Nevado, C. Angew. Chem., Int. Ed. 2014, 53, 5078 |
[3] | (b) Thaharn, W.; Soorukram, D.; Kuhakarn, C.; Tuchinda, P.; Reutrakul, V.; Pohmakotr, M. Angew. Chem., Int. Ed. 2014, 53, 2212; |
[3] | (c) Fuentes, N.; Kong, W.; Fernández-Sánchez, L.; Merino, E.; Nevado, C. J. Am. Chem. Soc. 2015, 137, 964; |
[3] | (d) Wu, X.; Zhu, C. Chin. J. Chem. 2019, 37, 171. |
[4] | Douglas, J. J.; Albright, H.; Sevrin, M. J.; Cole, K. P.; Stephenson, C. R . J.Angew. Chem., Int. Ed. 2015, 54, 14898. |
[5] | Benito Collado, A. B.; Diaz Buezo, N.; Jimenez-Aguado, A. M.; Lafuente Blanco, C.; Martinez-Grau, M. A.; Pedregal-Tercero, C.; Toledo Escribano, M. A. U.S. 8232289 B2, 2011. |
[6] | Douglas, J. J.; Sevrin, M. J.; Cole, K. P.; Stephenson, C. R . J.Org. Process Res. Dev. 2016, 20, 1148. |
[7] | Li, Y.; Hu, B.; Dong, W.; Xie, X.; Wan, J.; Zhang, Z . J. Org. Chem. 2016, 81, 7036. |
[8] | Alpers, D.; Cole, K. P.; Stephenson, C. R . J.Angew. Chem., Int. Ed. 2018, 57, 12167. |
[9] | Faderl, C.; Budde, S.; Kachkovskyi, G.; Rackl, D.; Reiser, O . J. Org. Chem. 2018, 83, 12192. |
[10] | Liu, C.; Zhang, B . RSC Adv. 2015, 5, 61199. |
[11] | Brachet, E.; Marzo, L.; Selkti, M.; K?nig, B.; Belmont, P . Chem. Sci. 2016, 7, 5002. |
[12] | Tang, S.; Yuan, L.; Deng, Y.-L.; Li, Z.-Z.; Wang, L.-N.; Huang, G.-X.; Sheng, R.-L . Tetrahedron Lett. 2017, 58, 329. |
[13] | Huang, H.; Li, Y . J. Org. Chem. 2017, 82, 4449. |
[14] | Monos, T. M.; McAtee, R. C.; Stephenson, C. R. J.Science 2018, 361, 1369. |
[15] | Zard, S. Z . Chem. Soc. Rev. 2008, 37, 1603. |
[16] | Yu, J.; Wu, Z.; Zhu, C . Angew. Chem., Int. Ed. 2018, 57, 17156. |
[17] | Whalley, D. M.; Duong, H. A.; Greaney, M. F . Chem. Eur. J. 2019, 25, 1927. |
[18] | Xu, P.; Hu, K.; Gu, Z.; Cheng, Y.; Zhu, C . Chem. Commun. 2015, 51, 7222. |
[19] | (a) Huang, H.-L.; Yan, H.; Yang, C.; Xia, W. Chem. Commun. 2015, 51, 4910 |
[19] | (b) Li, Y.; Liu, B.; Ouyang, X.-H.; Song, R.-J.; Li, J.-H. Org. Chem. Front. 2015, 2, 1457; |
[19] | (c) Cai, S.; Tian, Y.; Zhang, J.; Liu, Z.; Lu, M.; Weng, W.; Huang, M. Adv. Synth. Catal. 2018, 360, 4084; |
[19] | (d) Lu, M.; Qin, H.; Lin, Z.; Huang, M.; Weng, W.; Cai, S. Org. Lett. 2018, 20, 7611; |
[19] | (e) Wang, H.; Xu, Q.; Yu, S. Org. Chem. Front. 2018, 5, 2224; |
[19] | (f) Wang, Q.-L.; Chen, Z.; Zhou, C.-S.; Xiong, B.-Q.; Zhang, P.-L.; Yang, C.-A.; Liu, Y.; Zhou, Q. Tetrahedron Lett. 2018, 59, 4551; |
[19] | (g) Yin, Y.; Weng, W.-Z.; Sun, J.-G.; Zhang, B. Org. Biomol. Chem. 2018, 16, 2356; |
[19] | (h) Wei, X.-J.; No?l, T. J. Org. Chem. 2018, 83, 11377. 11377. |
[20] | Gu, L.; Gao, Y.; Ai, X.; Jin, C.; He, Y.; Li, G.; Yuan, M . Chem. Commun. 2017, 53, 12946. |
[21] | Zhou, N.-N.; Xu, P.; Li, W.-P.; Cheng, Y.-X.; Zhu, C.-J . Acta Chim. Sinica 2017, 75, 60. |
[21] | ( 周能能, 胥攀, 李伟鹏, 成义祥, 朱成建 , 化学学报, 2017, 75, 60.) |
[22] | Yu, J.; Wang, D.; Xu, Y.; Wu, Z.; Zhu, C . Adv. Synth. Catal. 2018, 360, 744. |
[23] | Tang, N.; Yang, S.; Wu, X.; Zhu, C . Tetrahedron 2019, 75, 1639. |
[24] | Wu, X.; Wang, M.; Huan, L.; Wang, D.; Wang, J.; Zhu, C . Angew. Chem. 2018, 130, 1656. |
[25] | Dondoni, A.; Marra, A . Chem. Rev. 2004, 104, 2557. |
[26] | Shu, W.; Genoux, A.; Li, Z.; Nevado, C . Angew. Chem., Int. Ed. 2017, 56, 10521. |
[27] | Wang, N.; Gu, Q.-S.; Li, Z.-L.; Li, Z.; Guo, Y.-L.; Guo, Z.; Liu, X.-Y . Angew. Chem., Int. Ed. 2018, 57, 14225. |
[28] | Wang, S.-F.; Cao, X.-P.; Li, Y . Angew. Chem., Int. Ed. 2017, 56, 13809. |
[29] | Gonzalez-Gomez, J. C.; Ramirez, N. P.; Lana-Villarreal, T.; Bonete, P. Org. Biomol. Chem. 2017, 15, 9680. |
[30] | Li, J.; Liu, Z.; Wu, S.; Chen, Y . Org. Lett. 2019, 21, 2077. |
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