Selenium-catalyzed oxidations with aqueous hydrogen peroxide. 2. Baeyer-Villiger reactions in homogeneous solution

Citation
Gj. Ten Brink et al., Selenium-catalyzed oxidations with aqueous hydrogen peroxide. 2. Baeyer-Villiger reactions in homogeneous solution, J ORG CHEM, 66(7), 2001, pp. 2429-2433
Citations number
31
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
JOURNAL OF ORGANIC CHEMISTRY
ISSN journal
00223263 → ACNP
Volume
66
Issue
7
Year of publication
2001
Pages
2429 - 2433
Database
ISI
SICI code
0022-3263(20010406)66:7<2429:SOWAHP>2.0.ZU;2-N
Abstract
Several diselenides were tested for catalytic activity in Baeyer-Villiger r eactions with 60% aqueous hydrogen peroxide. Bis [3,5-bis(trifluoromethyl)p henyl] diselenide forms the corresponding 3,5-bis(trifluoromethyl)benzene s eleninic acid in situ, which is a highly reactive and selective catalyst fo r the oxidation of carbonyl compounds in 1,1,1,3,3,3-hexafluoro-2-propanol, 2,2,2-trifluoroethanol,, or dichloromethane.