Photochemical strategies for carbon–heteroatom bond formation
Cavedon C, Seeberger PH, Pieber B. 2020. Photochemical strategies for carbon–heteroatom bond formation. European Journal of Organic Chemistry. 2020(10), 1379–1392.
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Author
Cavedon, Cristian;
Seeberger, Peter H.;
Pieber, BartholomäusISTA 
Abstract
Photochemistry enables new synthetic means to form carbon–heteroatom bonds. Photocatalysts can catalyze carbon–heteroatom cross-couplings by electron or energy transfer either alone or in combination with a second catalyst. Photocatalyst-free methods are possible using photolabile substrates or by generating photoactive electron donor-acceptor complexes. This review summarizes and discusses the strategies used in light-mediated carbon–heteroatom bond formations based on the proposed mechanisms.
Publishing Year
Date Published
2020-03-15
Journal Title
European Journal of Organic Chemistry
Volume
2020
Issue
10
Page
1379-1392
ISSN
eISSN
IST-REx-ID
Cite this
Cavedon C, Seeberger PH, Pieber B. Photochemical strategies for carbon–heteroatom bond formation. European Journal of Organic Chemistry. 2020;2020(10):1379-1392. doi:10.1002/ejoc.201901173
Cavedon, C., Seeberger, P. H., & Pieber, B. (2020). Photochemical strategies for carbon–heteroatom bond formation. European Journal of Organic Chemistry. Wiley. https://doi.org/10.1002/ejoc.201901173
Cavedon, Cristian, Peter H. Seeberger, and Bartholomäus Pieber. “Photochemical Strategies for Carbon–Heteroatom Bond Formation.” European Journal of Organic Chemistry. Wiley, 2020. https://doi.org/10.1002/ejoc.201901173.
C. Cavedon, P. H. Seeberger, and B. Pieber, “Photochemical strategies for carbon–heteroatom bond formation,” European Journal of Organic Chemistry, vol. 2020, no. 10. Wiley, pp. 1379–1392, 2020.
Cavedon C, Seeberger PH, Pieber B. 2020. Photochemical strategies for carbon–heteroatom bond formation. European Journal of Organic Chemistry. 2020(10), 1379–1392.
Cavedon, Cristian, et al. “Photochemical Strategies for Carbon–Heteroatom Bond Formation.” European Journal of Organic Chemistry, vol. 2020, no. 10, Wiley, 2020, pp. 1379–92, doi:10.1002/ejoc.201901173.
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