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Cite the Following Article
Stepwise radical cation Diels–Alder reaction via multiple pathways
Ryo Shimizu, Yohei Okada and Kazuhiro Chiba
Beilstein J. Org. Chem. 2018, 14, 704–708.
https://doi.org/10.3762/bjoc.14.59
How to Cite
Shimizu, R.; Okada, Y.; Chiba, K. Beilstein J. Org. Chem. 2018, 14, 704–708. doi:10.3762/bjoc.14.59
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- Heravi, M. M.; Zadsirjan, V.; Kouhestanian, E.; AlimadadiJani, B. Electrochemically Induced Diels‐Alder Reaction: An Overview. Chemical record (New York, N.Y.) 2019, 20, 273–331. doi:10.1002/tcr.201900018
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