Pitchumani, V and Ramamurthy, V (1994) Formation of rearrangement product in photolysis of α,α-dimethydeoxybenzoin upon cyclodextrin complexation. In: Photochemistry and photobiology, 59 (4). 399 -401 .
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Official URL: http://onlinelibrary.wiley.com/doi/10.1111/j.1751-...
Abstract
Solid-state irradiation of cyclodextrin complexes of alpha,alpha-dimethyldeoxybenzoin results in the formation of a significant amount of rearrangement product, 4-isopropylbenzophenone, in addition to cage products. This behavior is not observed in the photolysis in solution or in micellar media.
| Item Type: | Editorials/Short Communications |
|---|---|
| Additional Information: | Copyright of this article belongs to John Wiley and Sons. |
| Department/Centre: | Division of Chemical Sciences > Organic Chemistry |
| Date Deposited: | 27 May 2011 06:37 |
| Last Modified: | 27 May 2011 06:37 |
| URI: | http://eprints.iisc.ernet.in/id/eprint/36490 |
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