Mehta, Goverdhan ; Mohal, Narinder (1998) Baeyer-Villiger oxidation of norbornan-7-ones: long-range substituent effects on regioselectivity Journal of the Chemical Society, Perkin Transactions 1 (3). pp. 505-508. ISSN 0300-922X
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Official URL: http://pubs.rsc.org/en/Content/ArticleLanding/1998...
Related URL: http://dx.doi.org/10.1039/A706268K
Abstract
The regioselectivity of the Baeyer-Villiger oxidation of norbornan-7-ones can be steered by the distal 2-endo-substituents present. Hydrolysis of the resulting bicyclic lactones provides a stereospecific route to functionalized cyclohexanes.
| Item Type: | Article |
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| Source: | Copyright of this article belongs to Royal Society of Chemistry. |
| ID Code: | 29052 |
| Deposited On: | 18 Dec 2010 05:39 |
| Last Modified: | 17 May 2016 12:01 |
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