Biocatalytic, enantioenriched primary amination of tertiary C–H bonds
Author:
Funder
Foundation for the National Institutes of Health
Alexander von Humboldt-Stiftung
National Science Foundation
Publisher
Springer Science and Business Media LLC
Link
https://www.nature.com/articles/s41929-024-01149-w.pdf
Reference44 articles.
1. Chu, J. C. K. & Rovis, T. Complementary strategies for directed C(sp3)–H functionalization: a comparison of transition-metal-catalyzed activation, hydrogen atom transfer, and carbene/nitrene transfer. Angew. Chem. Int. Ed. 57, 62–101 (2018).
2. Dalton, T., Faber, T. & Glorius, F. C–H activation: toward sustainability and applications. ACS Cent. Sci. 7, 245–261 (2021).
3. Newton, C. G., Wang, S. G., Oliveira, C. C. & Cramer, N. Catalytic enantioselective transformations involving C–H bond cleavage by transition-metal complexes. Chem. Rev. 117, 8908–8976 (2017).
4. Saint-Denis, T. G., Zhu, R. Y., Chen, G., Wu, Q. F. & Yu, J. Q. Enantioselective C(sp3)–H bond activation by chiral transition metal catalysts. Science 359, eaao4798 (2018).
5. Rogge, T. et al. C–H activation. Nat. Rev. Methods Primers 1, 43 (2021).
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