75456-41-6Relevant academic research and scientific papers
PHENYLSELENENYL CHLORIDE IN ACETONITRILE-WATER; A HIGHLY CONVENIENT REAGENT FOR HYDROXYSELENATION OF OLEFINS AND PREPARATION OF CYCLIC ETHERS FROM DIENES
Toshimitsu, Akio,Aoai, Toshiaki,Owada, Hiroto,Uemura, Sakae,Okano, Masaya
, p. 5301 - 5306 (2007/10/02)
The reaction of phenylselenenyl chloride with olefins in aqueous acetonitrile affords β-hydroxyalkyl phenyl selenides in excellent yields, providing the most convenient method for hydroxyselenation of olefins so far reported.When the reaction was applied to conjugated dienes, monohydroxyselenated products were obtained in good to excellent yields.From non-conjugated dienes, on the other hand, cyclic ethers containing two phenylseleno groups were produced in good to excellent yields, the first step of this reaction being the hydroxyselenation of one double bond.
PHENYLSELENENYL CHLORIDE AS A REAGENT FOR THE FACILE PREPARATION OF CYCLIC ETHERS FROM DIOLEFINS
Uemura, Sakae,Toshimitsu, Akio,Aoai, Toshiaki,Okano, Masaya
, p. 1533 - 1536 (2007/10/02)
Various cyclic ethers are prepared in good to excellent yields by treating diolefins with phenylselenenyl chloride in aqueous acetonitrile.This is the most facile method for organoselenium-induced formation of cyclic ethers from diolefins so far reported.
