164403-41-2Relevant academic research and scientific papers
Reductive cleavage of the Se-Se bond by the Sm/CrCl3 system: A novel one-pot method for the synthesis of selenoesters
Liu, Yunkui,Zhang, Yongmin
, p. 4043 - 4049 (1999)
Diaryl diselenides can react with acid chlorides or acid anhydrides in one-pot by the Sm/CrCl3 system to give selenoesters in moderate to good yields under mild and neutral conditions.
Atom efficient preparation of zinc selenates for the synthesis of selenol esters under “On Water” conditions
Sancineto, Luca,Vargas, Jaqueline Pinto,Monti, Bonifacio,Arca, Massimiliano,Lippolis, Vito,Perin, Gelson,Lenardao, Eder Joao,Santi, Claudio
, (2017/06/29)
We describe here an atom efficient procedure to prepare selenol esters in good to excellent yields by reacting [(PhSe)2Zn] or [(PhSe)2Zn]TMEDA with acyl chlorides under “on water” conditions. The method is applicable to a series of aromatic and aliphatic acyl chlorides and tolerates the presence of other functionalities in the starting material.
Cleavage of Se-Se bond by Sm/cat.CoCl2 system: A facile and novel method for the preparation of selenoesters
Chen,Su
, p. 492 - 494 (2007/10/03)
The Sm/cat.CoCl2 system promoted diselenides to react with anhydrides or acyl chlorides to afford selenoesters in good yields under mild and neutral conditions.
Cleavage of Se-Se bond by Sm/cat. Cocl2 system: A novel method for the synthesis of selenoesters
Chen, Rener,Zhang, Yongmin
, p. 1331 - 1336 (2007/10/03)
The Sm/cat. COCl2 system promoted desalinates to react with anhydrides or acyl chlorides to afford selenoesters in good yield under mild and neutral conditions.
Reductive cleavage of Se - Si bond in arylselenotrimethylsilane: A novel method for the synthesis of selenoesters
Zhang,Zhang
, p. 3999 - 4002 (2007/10/03)
Arylselenotrimethylsilane is reduced by samarium diiodide to yield samarium arylselenolates. These new selenolate anion species reacted smoothly with acyl halides to give selenoesters.
