Singh, Anil K. ; Sonar, Sanjay M. (1985) Photorearrangement of aryl esters in micellar medium Synthetic Communications, 15 (12). pp. 1113-1121. ISSN 0039-7911
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Official URL: http://www.tandfonline.com/doi/abs/10.1080/0039791...
Related URL: http://dx.doi.org/10.1080/00397918508076851
Abstract
Effect of a micelle (SDS) on the photorearrangement of aryl esters have been investigated. Thus, phenyl, p- and m-cresyl, and 2-naphthyl benzoates yielded the corresponding o-hydroxybenzophenones as a major product in high yield. Phenyl cinnamate gave 2-hydroxychalcone. 2,4,6-Tri-butylphenylbenzoate, however, underwent decarboxylation yielding 2,4,6-tri-t-butyl biphenyl in quantitative yield.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Taylor and Francis Group. |
| ID Code: | 54120 |
| Deposited On: | 11 Aug 2011 11:43 |
| Last Modified: | 11 Aug 2011 11:43 |
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