References
- Wirth, T.; Kita, Y.; Wirth, T. Hypervalent Iodine Chemistry. Springer: Cham, 2016; Vol. 373.
- (a) Spyroudis, S.; Tarantili, P. J. Org. Chem. 1993, 58, 4885–4889. DOI: 10.1021/jo00070a025. (b) Zhdankin, V. V.; Stang, P. J. Chem. Rev. 2008, 108, 5299–5358. DOI: 10.1021/cr800332c. (c) Moriarty, R. M.; Tyagi, S.; Ivanov, D.; Constantinescu, M. J. Am. Chem. Soc. 2008, 130, 7564–7565. DOI: 10.1021/ja802735f. (d) Yoshimura, A.; Zhdankin, V. V. Chem. Rev. 2016, 116, 3328–3435. DOI: 10.1021/acs.chemrev.5b00547. (e) Zhao, Z.; Luo, Y.; Liu, S.; Zhang, L.; Feng, L.; Wang, Y. Angew. Chem. Int. Ed. 2018, 57, 3792–3796. DOI: 10.1002/anie.201800389. (f) Murphy, G. K.; Racicot, L.; Carle, M. S. Asian J. Org. Chem. 2018, 7, 837–851. DOI: 10.1002/ajoc.201800058. (g) Chidley, T.; Jameel, I.; Rizwan, S.; Peixoto, P. A.; Pouységu, L.; Quideau, S.; Hopkins, W. S.; Murphy, G. K. Angew. Chem. Int. Ed. Engl. 2019, 58, 16959–16965. DOI: 10.1002/anie.201908994. (h) Jiang, Y.; Li, P.; Zhao, J.; Liu, B.; Li, X. Org. Lett. 2020, 22, 7475–7479. DOI: 10.1021/acs.orglett.0c02618. (i) Yang, L.; Pi, C.; Wu, Y.; Cui, X. Org. Lett. 2022, 24, 7502–7506. DOI: 10.1021/acs.orglett.2c02660. (j) Ren, J.; Pi, C.; Cui, X.; Wu, Y. Green Chem. 2022, 24, 3017–3022. DOI: 10.1039/D1GC04825B. (k) Mi, X.; Pi, C.; Feng, W.; Cui, X. Org. Chem. Front. 2022, 9, 6999–7015. DOI: 10.1039/D2QO01332K.
- Chen, Z. H.; Tu, Y. Q.; Zhang, S. Y.; Zhang, F. M. Org. Lett. 2011, 13, 724–727. DOI: 10.1021/ol102955e.
- Wang, Y.; Chen, C.; Peng, J.; Li, M. Angew. Chem. Int. Ed. Engl. 2013, 52, 5323–5327. DOI: 10.1002/anie.201300586.
- Yang, B.; Yu, D.; Xu, X. H.; Qing, F. L. ACS Catal. 2018, 8, 2839–2843. DOI: 10.1021/acscatal.7b03990.
- (a) Dess, D. B.; Martin, J. C. J. Am. Chem. Soc. 1991, 113, 7277. DOI: 10.1021/ja00019a027. (b) Frigerio, M.; Santagostino, M.; Sputore, S. J. Org. Chem. 1999, 64, 4537–4538. DOI: 10.1021/jo9824596.
- (a) Yue, Q.; Yang, T.; Yang, Y.; Zhang, C.; Zhang, Q.; Li, D. Asian J. Org. Chem. 2017, 6, 936–942. DOI: 10.1002/ajoc.201700163. (b) Jeyakannu, P.; Chandru Senadi, G.; Chiang, C. ‐H.; Kumar Dhandabani, G.; Chang, Y.‐C.; Wang, J. ‐J. Adv. Synth. Catal. 2020, 362, 2911–2920. DOI: 10.1002/adsc.202000402.
- Li, B.; Yuan, J.; Ye, X.; Zhang, R.; Li, J.; Wang, Y.; Hu, J.; Dong, D. J. Org. Chem. 2021, 86, 17944–17954. DOI: 10.1021/acs.joc.1c02276.
- Tsai, C. H.; Reddy, D. M.; Hsieh, P. A.; Liu, Y. C.; Kandasamy, M.; Lin, W. Y.; Lee, C. F. Synthesis 2016, 48, 2781–2788. DOI: 10.1055/s-0036-1588070.
- Rattanangkool, E.; Krailat, W.; Vilaivan, T.; Phuwapraisirisan, P.; Sukwattanasinitt, M.; Wacharasindhu, S. Eur. J. Org. Chem. 2014, 2014, 4795–4804. DOI: 10.1002/ejoc.201402180.
- Zhou, Q.-Z.; He, C.-L.; Chen, Z.-C. Chin. J. Org. Chem. 2008, 28, 1097.
- Eljo, J.; Carle, M. S.; Murphy, G. K. Synlett 2017, 28, 2871–2875. DOI: 10.1055/s-0036-1589069.
- Kaushik, C.; Pahwa, A.; Kumar, D.; Kumar, A.; Singh, D.; Kumar, K.; Luxmi, R. J. Heterocyclic Chem. 2018, 55, 1720–1728. DOI: 10.1002/jhet.3209.
- Chen, S. H.; Wei, J. M.; Farina, V. Tetrahedron Lett 1993, 34, 3205–3206. DOI: 10.1016/S0040-4039(00)73661-6.
- Li, D.; Wang, Y.; Zhang, Q. Preparation Method and Device for Iodobenzene Dibenzoate derivative. Patent CN106278899A, 2017.
- (a) Gawne, G.; Kenner, G. W.; Sheppard, R. C. J. Am. Chem. Soc. 1969, 91, 5669–5671. DOI: 10.1021/ja01048a057. (b) McNulty, J.; Capretta, A.; Laritchev, V.; Dyck, J.; Robertson, A. J. Angew Chem. Int. Ed. Engl. 2003, 42, 4051–4054. DOI: 10.1002/anie.200351209.
- See in the Supporting Information.
- Nicolaou, K. C.; Mathison, C. J. N.; Montagnon, T. J. Am. Chem. Soc. 2004, 126, 5192–5201. DOI: 10.1021/ja0400382.