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1996 rearrangements rearrangements O 0140 28 - 056 Electrooxidative Pinacol-Type Rearrangement of β-Hydroxy Sulfides. Efficient C-S Cleavage Mediated by Chloride Ion Oxidation. It offers a new method to prepare 2-phenyl substituted ketones like ( II), (IV), and (VII). — (KIMURA, M.; KOBAYASHI, K.; YAMAMOTO, Y.; SAWAKI, Y.; Tetrahedron 52 (1996) 12, 4303-4310; Dep. Appl. Chem., Fac. Eng., Nagoya Univ., Chikusa, Nagoya 464-01, Japan; EN) 1

ChemInform Abstract: Electrooxidative Pinacol-Type Rearrangement of β-Hydroxy Sulfides. Efficient C-S Cleavage Mediated by Chloride Ion Oxidation

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Page 1: ChemInform Abstract: Electrooxidative Pinacol-Type Rearrangement of β-Hydroxy Sulfides. Efficient C-S Cleavage Mediated by Chloride Ion Oxidation

1996 rearrangements

rearrangementsO 0140

28 - 056Electrooxidative Pinacol-Type Rearrangement of β-Hydroxy Sulfides.Efficient C-S Cleavage Mediated by Chloride Ion Oxidation. — Itoffers a new method to prepare 2-phenyl substituted ketones like ( II), (IV), and(VII). — (KIMURA, M.; KOBAYASHI, K.; YAMAMOTO, Y.; SAWAKI, Y.;Tetrahedron 52 (1996) 12, 4303-4310; Dep. Appl. Chem., Fac. Eng., NagoyaUniv., Chikusa, Nagoya 464-01, Japan; EN)

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