Enantioconvergent and regioselective reductive coupling of propargylic esters with chlorogermanes by nickel catalysis
Author:
Funder
National Natural Science Foundation of China
Fundamental Research Funds for the Central Universities
Publisher
Springer Science and Business Media LLC
Subject
Process Chemistry and Technology,Biochemistry,Bioengineering,Catalysis
Link
https://www.nature.com/articles/s41929-023-01052-w.pdf
Reference54 articles.
1. Cherney, A. H., Kadunce, N. T. & Reisman, S. E. Enantioselective and enantiospecific transition-metal-catalyzed cross-coupling reactions of organometallic reagents to construct C–C bonds. Chem. Rev. 115, 9587–9652 (2015).
2. Fu, G. C. Transition-metal catalysis of nucleophilic substitution reactions: a radical alternative to SN1 and SN2 processes. ACS Cent. Sci. 3, 692–700 (2017).
3. Lucas, E. L. & Jarvo, E. R. Stereospecific and stereoconvergent cross-couplings between alkyl electrophiles. Nat. Rev. Chem. 1, 0065 (2017).
4. Poremba, K. E., Dibrell, S. E. & Reisman, S. E. Nickel-catalyzed enantioselective reductive cross-coupling reactions. ACS Catal. 10, 8237–8246 (2020).
5. Goldfogel, M. J., Huang, L. & Weix, D. J. in Nickel Catalysis in Synthesis: Methods and Reactions (ed. Ogoshi, S.) 183–222 (Wiley-VCH, 2020).
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