Publication Cover
Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 15, 1985 - Issue 12
70
Views
14
CrossRef citations to date
0
Altmetric
Original Articles

Photorearrangement of Aryl Esters in Micellar Medium

&
Pages 1113-1121 | Published online: 19 Dec 2006
 

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.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.