Bhaduri, Sumit ; Sharma, Krishna ; Mukesh, Doble (1993) Transfer hydrogenation of ketones with [Ru4H3(CO)12]- as the precatalyst Journal of the Chemical Society Dalton Transactions . pp. 1191-1199. ISSN 1472-7773
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Official URL: http://www.rsc.org/Publishing/Journals/DT/article....
Related URL: http://dx.doi.org/10.1039/DT9930001191
Abstract
The cluster [N(PPh3)2][Ru4H3(CO)12]1a has been found to be an efficient precatalyst for the transfer hydrogenations of ketones and α,β-unsaturated ketones. With substrates such as (5S)-carvone [2-methyl-5-(1-methylethenyl)cyclohex-2-en-1-one], (3R)-methylcyclopentanone and (3R)-methylcyclohexanone, moderate to high diastereoselectivities were observed for reduction of the conjugated olefinic and ketonic functionalities respectively. Aromatisation of carvone to 5-isopropyl-2-methylphenol and disproportionation of cyclohex-2-en-1-one to phenol and cyclohexanone have also been found to be catalysed by 1a. Studies with radical inhibitors and other evidence suggest a radical mechanism for the transfer-hydrogenation and aromatisation reactions. In the transfer hydrogenation of cyclohex-2-en-1-one, the rate of conversion of 1a into other soluble species can be modelled accurately if autocatalysis is assumed. The time-dependent concentration profiles of cyclohex-2-en-1-one, cyclohexanone and cyclohexanol are simulated well if autocatalytic formation of an active intermediate followed by consecutive reactions leading to the formation of products is assumed. Such a model is also consistent with the proposed radical mechanism.
Item Type: | Article |
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Source: | Copyright of this article belongs to Royal Society of Chemistry. |
ID Code: | 2163 |
Deposited On: | 08 Oct 2010 07:41 |
Last Modified: | 08 Oct 2010 07:41 |
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