Computational Prediction of One-Step Synthesis of Seven-membered Fused Rings by (5+2) Cycloaddition Utilising Cycloalkenes
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/srep12272.pdf
Reference50 articles.
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3. Ovaska, T. V., Sullivan, J. A., Ovaska, S. I., Winegrad, J. B. & Fair, J. D. Asymmetric synthesis of seven-membered carbocyclic rings via a sequential oxyanionic 5-exo-dig cyclization/claisen rearrangement process. total synthesis of (−)-frondosin B. Org. Lett. 11, 2715–2718 (2009).
4. Sarpong, R., Su, J. T. & Stoltz, B. M. The development of a facile tandem Wolff/Cope rearrangement for the synthesis of fused carbocyclic skeletons. J. Am. Chem. Soc. 125, 13624–13625 (2003).
5. Brookhart, M., Davis, E. R. & Harris, D. L. Low-temperature protonation of cyclooctatetraeneiron tricarbonyl and methylcyclooctatetraeneiron tricarbonyl. Generation and observation of cyclooctatrienyliron tricarbonyl cations. J. Am. Chem. Soc. 94, 7853–7858 (1972).
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