The high stability of aromatic compounds often limits the types of reaction that can be conducted on them. Now, a series of photochemically promoted addition reactions has been used to effect the oxidative dearomatization of benzene derivatives. These reactions provide a suite of versatile new building blocks for chemical synthesis.
References
Lloyd, D. Non-Benzenoid Conjugated Carbocyclic Compounds 1–16 (Elsevier, 1984).
Francl, M. Nat. Chem. 7, 6–7 (2015).
Zhuo, C.-X., Zheng, C. & You, S.-L. Acc. Chem. Res. 47, 2558–2573 (2014).
You, S.-L. (ed) Asymmetric Dearomatization Reactions (Wiley, 2016).
Rickards, R. W. & Cornforth, J. Biogr. Mems Fell. R. Soc. 53, 21–44 (2007).
Lewis, S. E. Chem. Commun. 50, 2821–2830 (2014).
Hamrock, S. J. & Sheridan, R. S. J. Am. Chem. Soc. 111, 9247–9249 (1989).
Southgate, E. H., Pospech, J., Fu, J., Holycross, D. R. & Sarlah, D. Nat. Chem. 8, 922–928 (2016).
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Banwell, M. A light touch breaks a strong ring. Nature Chem 8, 900–901 (2016). https://doi.org/10.1038/nchem.2623
Published:
Issue Date:
DOI: https://doi.org/10.1038/nchem.2623
- Springer Nature Limited