1036648-28-8Relevant articles and documents
Toluates: unexpectedly versatile reagents
Lam, Kevin,Markó, István E.
experimental part, p. 10930 - 10940 (2010/02/28)
The mechanism of the monoelectronic reduction of aromatic esters has been investigated. The unexpected synthetic utility of the toluate moiety in the deoxygenation of alcohols and the allylation of ketones is also reported. Finally, the use of aromatic esters as robust, though easily removable, protecting groups is depicted.
Using toluates as simple and versatile radical precursors
Lam, Kevin,Marko, Istvan E.
supporting information; experimental part, p. 2773 - 2776 (2009/05/30)
(Chemical Equation Presented) The viability of the toluate moiety as a radical precursor has been examined by studying deoxygenation and cyclization reactions.