Palladium-Mediated Ring Opening of Hydroxycyclopropanes
Organic Letters1999Vol. 2(2), pp. 147–149
Citations Over TimeTop 13% of 1999 papers
Abstract
[reaction: see text] The palladium-mediated ring opening of substituted cyclopropanols has been found to take place predominantly at the less substituted C-C bond. Thus, sequential application of the titanium-mediated cyclopropanation of esters and the palladium-mediated ring opening of the resulting cyclopropanols provides a convenient method for functionalizing monosubstituted olefins.
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