Diaklylaluminum chloride catalyzed ene reactions of aldehydes. Synthesis of ipsenol

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Abstract

Dimethylaluminum chloride which is a mild Lewis acid and a proton scavenger, catalyzes the ene reactions of aliphatic and aromatic aldehydes. Proton initiated rearrangements do not occur, since the alcohol-Lewis acid complex formed in the ene reaction rapidly to give methane and a non-acidic aluminum alkoxide. © 1980.

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Snider, B. B., & Rodini, D. J. (1980). Diaklylaluminum chloride catalyzed ene reactions of aldehydes. Synthesis of ipsenol. Tetrahedron Letters, 21(19), 1815–1818. https://doi.org/10.1016/S0040-4039(00)92787-4

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