Mild construction of N-fused polycyclic compounds via Rh(III)/EosinY co-catalyze C−H activation

Green Synthesis and Catalysis - 2022
Zhouping Wu1, Guanghui Lv2, Zheng Lin1, Jiangyan Tang3, Jian Chen1, Jianghong Liu3, Li Hai3, Yong Wu3
1Key Laboratory of Drug Targeting and Drug Delivery System of the Education Ministry and Sichuan Province, Sichuan Engineering Laboratory for Plant Sourced Drug and Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy, Sichuan University, Chengdu, 610041 China
2Department of Pharmacy, Taihe Hospital, Hubei University of Medicine, No. 32 South Renmin Road, Shiyan, 442000, China
3Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry and Sichuan Province, Sichuan Engineering Laboratory for Plant-Sourced Drug and Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy, Sichuan University, Chengdu 610041, China

Tài liệu tham khảo

Ros, 2014, Chem. Soc. Rev., 43, 3229, 10.1039/C3CS60418G Sambiagio, 2018, Chem. Soc. Rev., 47, 6603, 10.1039/C8CS00201K Najera, 2019, Chem. Soc. Rev., 48, 4515, 10.1039/C8CS00872H Hartwig, 2016, J. Am. Chem. Soc., 138, 2, 10.1021/jacs.5b08707 Lam, 2021, Angew. Chem., Int. Ed., 60, 15767, 10.1002/anie.202011901 Ghosh, 2020, Org. Lett., 22, 3547, 10.1021/acs.orglett.0c00975 Aslam, 2021, Org. Lett., 23, 6206, 10.1021/acs.orglett.1c01793 Nguyen, 2016, Chem. Commun., 52, 4914, 10.1039/C6CC01436D Rago, 2021, Green Synthesis and Catalysis, 2, 216, 10.1016/j.gresc.2021.02.001 Jia, 2016, Angew. Chem., Int. Ed., 55, 9134, 10.1002/anie.201508119 Bergstrom, 2021, Angew. Chem. Int. Ed., 60, 6864, 10.1002/anie.202007001 Xiang, 2019, Adv. Synth. Catal., 361, 919, 10.1002/adsc.201800960 Tang, 2018, Org. Chem. Front., 5, 2583, 10.1039/C8QO00619A Mai, 2018, Chem. Commun., 54, 10240, 10.1039/C8CC05390A Li, 2020, Org. Chem. Front., 7, 919, 10.1039/D0QO00073F Li, 2019, Org. Biomol. Chem., 17, 9140, 10.1039/C9OB01744E Li, 2016, Adv. Synth. Catal., 358, 880, 10.1002/adsc.201500709 Green, 2020, Org. Process Res. Dev., 24, 67, 10.1021/acs.oprd.9b00422 Yoshimura, 2016, Chem. Rev., 116, 3328, 10.1021/acs.chemrev.5b00547 Muller, 2004, Acc. Chem. Res., 37, 243, 10.1021/ar0202619 Antos, 2012, J. Org. Chem., 77, 10949, 10.1021/jo3020787 Chelli, 2016, J. Am. Chem. Soc., 138, 10304, 10.1021/jacs.6b05768 Jiang, 2020, Org. Lett., 22, 7475, 10.1021/acs.orglett.0c02618 Mayakrishnan, 2020, Chem. Commun., 56, 15462, 10.1039/D0CC06038K Nunewar, 2021, Org. Lett., 23, 4233, 10.1021/acs.orglett.1c01167 Kumar, 2021, Asian J. Org. Chem., 11 Nunewar, 2022, Chem. Commun., 58, 6140, 10.1039/D2CC01386J Li, 2022, Org. Chem. Front., 9, 2181, 10.1039/D2QO00144F Li, 2022, J. Org. Chem., 87, 8142, 10.1021/acs.joc.2c00852 Kharitonov, 2022, Coord. Chem. Rev., 471, 10.1016/j.ccr.2022.214744 Skubi, 2016, Chem. Rev., 116, 10035, 10.1021/acs.chemrev.6b00018 Fabry, 2016, Acc. Chem. Res., 49, 1969, 10.1021/acs.accounts.6b00275 De Abreu, 2020, Eur. J. Org. Chem., 2020, 1327, 10.1002/ejoc.201901146 Sen, 2020, J. Org. Chem., 85, 15287, 10.1021/acs.joc.0c02120 Fabry, 2014, Angew. Chem. Int. Ed., 53, 10228, 10.1002/anie.201400560 Kalyani, 2011, J. Am. Chem. Soc., 133, 18566, 10.1021/ja208068w Baviskar, 2015, ACS Med. Chem. Lett., 6, 481, 10.1021/acsmedchemlett.5b00040 Wang, 2019, Eur. J. Med. Chem., 178, 715, 10.1016/j.ejmech.2019.06.038 Palmer, 2007, J. Med. Chem., 50, 6240, 10.1021/jm7010063 Chen, 2022, Org. Biomol. Chem., 20, 887, 10.1039/D1OB02110A
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Green Synthesis and Catalysis

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