Heathcote, David M., De Boos, Gareth A., Atherton, John H. and Page, Michael I. (1998) Mechanism of hydrolysis of coumaran-2-ones. Journal of the Chemical Society, Perkin Transactions 2 (3). pp. 535-540. ISSN 1472-779XMetadata only available from this repository.
The hydrolysis of coumaran-2-one and 5-substituted 3-phenylcoumaran-2-ones is preceded by a pre-equilibrium involving the formation of an enolate anion at high pH. The pKa of 3-phenylcoumaran-2-one is 8.39 in water at 25 °C and the 3-phenyl substituent increases the carbon acidity by 104. However, despite this ready carbanion formation, the conventional addition–elimination mechanism for hydrolysis of 3-phenylcoumaran-2-ones is confirmed by a solvent kinetic isotope effect of 0.63 and a Brønsted 1g of –0.6. This is compatible with rate limiting formation of a tetrahedral intermediate.
|Subjects:||Q Science > Q Science (General)|
Q Science > QD Chemistry
|Schools:||School of Applied Sciences|
|Depositing User:||Sharon Beastall|
|Date Deposited:||05 Nov 2009 11:47|
|Last Modified:||05 Nov 2009 11:47|
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