1169497-02-2Relevant articles and documents
Synthesis of selenol esters from diorganyl diselenides and acyl chlorides under solvent-free conditions and microwave irradiation
Godoi, Marcelo,Ricardo, Eduardo W.,Botteselle, Giancarlo V.,Galetto, Fabio Z.,Azeredo, Juliano B.,Braga, Antonio L.
, p. 456 - 460 (2012)
Herein, we report an efficient, quick and eco-friendly new method for the synthesis of a variety of selenol esters. This novel solvent-free methodology gave good to excellent isolated yields of desired products after just 2 min under microwave irradiation
Ionic liquid: An efficient and reusable media for seleno- and thioester synthesis promoted by indium
Tabarelli, Greice,Alberto, Eduardo E.,Deobald, Anna M.,Marin, Graciane,Rodrigues, Oscar E.D.,Dornelles, Luciano,Braga, Antonio L.
experimental part, p. 5728 - 5731 (2010/11/16)
A series of thio and selenoesters were efficiently obtained employing stable diorganyl chalcogenides, acyl chlorides, and In as reducing agent in BMIM·PF6. Recycling of the ionic liquid was also performed, which was reused three times.
Efficient synthesis of selenol esters from acid chlorides mediated by indium metal
Marin, Graciane,Braga, Antonio L.,Rosa, Anderson S.,Galetto, Fábio Z.,Burrow, Robert A.,Gallardo, Hugo,Paix?o, Marcio W.
supporting information; experimental part, p. 4614 - 4618 (2009/10/02)
This article describes an efficient and easy one-pot route for the synthesis of a wide range of selenol esters from acyl chloride with diselenides in the presence of indium metal. A variety of functional groups can be tolerated within the diorgano diselenide and the acyl chloride coupling partner.