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 .Full text not available from this repository.
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|
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