Abstract
An efficient method was developed for the synthesis of highly substituted naphthalenes through rhodium-catalyzed oxidative benzannulation of N-pivaloylanilines with internal alkynes. The benzannulation reaction proceeded smoothly through dual C−H bond activation to produce the corresponding highly substituted naphthalene products in satisfactory to good yields.
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Zhang, X., Yu, X., Feng, X., Yamamoto, Y., Almansour, A. I., Arumugam, N., … Bao, M. (2016). Rhodium-Catalyzed Oxidative Benzannulation of N-Pivaloylanilines with Internal Alkynes through Dual C−H Bond Activation: Synthesis of Highly Substituted Naphthalenes. Chemistry - An Asian Journal, 11(22), 3241–3250. https://doi.org/10.1002/asia.201601131
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