Synthesis of α-aryl ketones through transition-metal-free cross-coupling
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Publisher
Springer Science and Business Media LLC
Link
https://www.nature.com/articles/s44160-023-00374-8.pdf
Reference5 articles.
1. Miyaura, N. & Suzuki, A. Palladium-catalyzed cross-coupling reactions of organoboron compounds. Chem. Rev. 95, 2457–2483 (1995). A review article that presents Suzuki cross-coupling.
2. Kambe, N., Iwasaki, T. & Terao, J. Pd-catalyzed cross-coupling reactions of alkyl halides. Chem. Soc. Rev. 40, 4937–4947 (2011). A review article that presents the difficulties and progress of palladium-promoted coupling reactions involving C(sp3)–X bonds.
3. Yang, K. & Song, Q. Tetracoordinate boron intermediates enable unconventional transformations. Acc. Chem. Res. 54, 2298–2312 (2021). A review article that presents our research on the chemistry of tetracoordinate boron intermediates.
4. Yang, K. et al. Passerini-type reaction of boronic acids enables α-hydroxyketones synthesis. Nat. Commun. 12, 441 (2021). This paper reports several 1,4-metallate migrations of tetracoordinate boron intermediates.
5. He, Z., Song, F., Sun, H. & Huang, Y. Transition-metal-free Suzuki-type cross-coupling reaction of benzyl halides and boronic acids via 1,2-metalate shift. J. Am. Chem. Soc. 140, 2693–2699 (2018). This paper explains the migration ability of different boronic acids.
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