Rao, V Jayathirtha and Muthuramu, K and Ramamurthy, V (1982) Oxidations of thio ketones by singlet and triplet oxygen. In: Journal of Organic Chemistry, 47 (1). pp. 127-131.
fultext.pdf - Published Version
Restricted to Registered users only
Download (628Kb) | Request a copy
Oxidation of di-tert-butyl thioketone (1) and 2,2,4,4-tetramethylcyclobutylth ioketone (2) by singlet oxygen yields the corresponding sulfine and ketone; in the case of 1 the sulfine is the major product, whereas in 2 it is the ketone. 1,2,3-Dioxathietane has been suggested as the precursor for the ketones, and the zwitterionic/diradid peroxide is believed to be a common primary intermediate for both sulfine and ketone. Steric influence is felt both during primary interaction between singlet oxygen and thioketone and during the partitioning of the peroxide intermediate. Steric interaction is suggested as the reason for variations in the product distribution between 1 and 2. Singlet oxygen is also generated through energy transfer from the triplet state of thioketones. These excited states also directly react with oxygen to yield ketone.
|Item Type:||Journal Article|
|Additional Information:||Copyright of this article belongs to American Chemical Society.|
|Department/Centre:||Division of Chemical Sciences > Organic Chemistry|
|Date Deposited:||14 Dec 2009 06:00|
|Last Modified:||19 Sep 2010 05:47|
Actions (login required)