One-electron reductive intramolecular cyclization of enones with ketones or aldehydes mediated by samarium diiodide and electrolysis to afford cis-trimethylhydrindanolones. The reactions gave selectivities ranging from 1:1 to 100:0 depending on the conditions. © 2012 by the authors.
CITATION STYLE
Sono, M., Ise, N., Shoji, T., & Tori, M. (2012). Cyclizations producing hydrindanones with two methyl groups at the juncture positions mediated by samarium diiodide and electrolysis. Molecules, 17(9), 11079–11088. https://doi.org/10.3390/molecules170911079
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