Cascade radical reaction of substrates with a carbon–carbon triple bond as a radical acceptor

Scholarly Works

• Rosenstein, I. J. doi:10.1002/0471264180.or110.01
• Sahharova, L. T.; Gordeev, E. G.; Eremin, D. B.; Ananikov, V. P. Computational Design of Radical Recognition Assay with the Possible Application of Cyclopropyl Vinyl Sulfides as Tunable Sensors. International journal of molecular sciences 2021, 22, 7637. doi:10.3390/ijms22147637
• Zhu, S.; Cheng, Q.; Yang, H.; Chen, X.; Han, Y.; Yan, C.-G.; Shi, Y.-C.; Hou, H. Three-Component Radical Iodonitrosylative Cyclization of 1,6-Enynes under Metal-Free Conditions. Organic letters 2021, 23, 5044–5048. doi:10.1021/acs.orglett.1c01576
• Dong, M.; Wang, D.; Tong, X. PhI(OAc)2-Mediated Dihalogenative Cyclization of 1,6-Enyne with Lithium Halide. Organic letters 2021, 23, 3588–3592. doi:10.1021/acs.orglett.1c00987
• Miyabe, H. Synthetic Approaches to Nonaromatic Nitrogen Heterocycles; Wiley, 2020; pp 595–629. doi:10.1002/9781119708841.ch19
• Takahashi, T.; Kurahashi, T.; Matsubara, S. Nickel-Catalyzed Intermolecular Carbobromination of Alkynes. ACS Catalysis 2020, 10, 3773–3777. doi:10.1021/acscatal.0c00980
• Gao, L.-H.; Zhang, J.-Y.; Song, S.-Z.; Cao, T.-T.; Ge, G.-P.; Li, Q.; Wei, W.-T. Base-promoted domino radical cyclization of 1,6-enynes. Organic & biomolecular chemistry 2019, 17, 7674–7678. doi:10.1039/c9ob01550g
• Mishra, M.; Mohapatra, S.; Mishra, N. P.; Jena, B. K.; Panda, P.; Nayak, S. Recent advances in iron(III) chloride catalyzed synthesis of heterocycles. Tetrahedron Letters 2019, 60, 150925. doi:10.1016/j.tetlet.2019.07.016
• Buttard, F.; Berthonneau, C.; Hiebel, M.-A.; Brière, J.-F.; Suzenet, F. Organocatalytic aza-Michael Reaction to 3-Vinyl-1,2,4-triazines as a Valuable Bifunctional Platform. The Journal of organic chemistry 2019, 84, 3702–3714. doi:10.1021/acs.joc.9b00141
• Meazza, M.; Companyó, X.; Rios, R. Syntheses of Lactams by Tandem Reactions. Asian Journal of Organic Chemistry 2018, 7, 1934–1956. doi:10.1002/ajoc.201800300
• Miyabe, H.; Kawashima, A.; Yoshioka, E.; Kohtani, S. Progress in Enantioselective Radical Cyclizations. Chemistry (Weinheim an der Bergstrasse, Germany) 2017, 23, 6225–6236. doi:10.1002/chem.201603124
• Hu, M.; Song, R.-J.; Ouyang, X.-H.; Tan, F.-L.; Wei, W.-T.; Li, J.-H. Copper-catalyzed oxidative [2+2+1] annulation of 1,n-enynes with α-carbonyl alkyl bromides through C–Br/C–H functionalization. Chemical communications (Cambridge, England) 2016, 52, 3328–3331. doi:10.1039/c5cc10132h
• Hu, M.; Liu, B.; Ouyang, X.-H.; Song, R.-J.; Li, J.-H. Nitrative Cyclization of 1‐Ethynyl‐2‐(vinyloxy)benzenes to Access 1‐[2‐(Nitromethyl)benzofuran‐3‐yl] Ketones Through Dioxygen Activation. Advanced Synthesis & Catalysis 2015, 357, 3332–3340. doi:10.1002/adsc.201500336
• Che, C.; Zheng, H.; Zhu, G. Copper-Catalyzed trans -Carbohalogenation of Terminal Alkynes with Functionalized Tertiary Alkyl Halides. Organic letters 2015, 17, 1617–1620. doi:10.1021/acs.orglett.5b00546
• Miyabe, H.; Yoshioka, E.; Kohtani, S. Research and Development of Domino Radical Cyclization Reactions. Journal of Synthetic Organic Chemistry, Japan 2015, 73, 895–901. doi:10.5059/yukigoseikyokaishi.73.895
• Xu, T.; Hu, X. Copper‐Catalyzed 1,2‐Addition of α‐Carbonyl Iodides to Alkynes. Angewandte Chemie 2014, 127, 1323–1327. doi:10.1002/ange.201410279
• Xu, T.; Hu, X. Copper‐Catalyzed 1,2‐Addition of α‐Carbonyl Iodides to Alkynes. Angewandte Chemie (International ed. in English) 2014, 54, 1307–1311. doi:10.1002/anie.201410279
• Tang, Y.; Liu, J.-t.; Chen, P.; Lv, M.; Wang, Z.; Huang, Y. Protecting-Group-Free Total Synthesis of Aplykurodinone-1. The Journal of organic chemistry 2014, 79, 11729–11734. doi:10.1021/jo501684k
• Miyabe, H.; Takemoto, Y. Cascade radical reactions via carbon-carbon/heteroatom bond-forming process. Universal Organic Chemistry 2014, 2, 1. doi:10.7243/2053-7670-2-1
• Stephenson, C. R. J.; Studer, A.; Curran, D. P. The renaissance of organic radical chemistry - deja vu all over again. Beilstein journal of organic chemistry 2013, 9, 2778–2780. doi:10.3762/bjoc.9.312

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