118989-25-6Relevant articles and documents
Phenylselenoetherification of Some Δ5-Alkenols in the Presence of Pyridine, Ag2O, and AgOAc as Additives
Bugar?i?, Zorica M.,Gavrilovi?, Marijana
, p. 1359 - 1363 (2003)
An improved procedure for intramolecular cyclization of some Δ 5-aikenols using PhSeX (X=Cl, Br) was developed. We found that cyclization can be facilitated in the presence of pyridine, Ag2O, and AgQAc as additives. Thus, a catalytic
Regioselectivity in Cyclofunctionalization of Olefinic Alcohols with Benzeneselenenyl Halides at Different Temperatures
Konstantinovic, Stanimir,Bugarcic, Zorica,Milosavljevic, Slobodan,Schroth, Gerhard,Mihailovic, Mihailo Lj.
, p. 261 - 268 (2007/10/02)
The regioselectivity in cyclofunctionalization of some acyclic olefinic alcohols with benzeneselenenyl halides (PhSeCl and PhSeBr) at different temperatures (-78 deg C, 0 deg C and room temperature) is investigated.It has been found that Δ4- and Δ5-alkenols are converted into five- and/or six-membered cyclic phenyl selenoethers, the yield of which decreases with increasing temperature.PhSeCl has been found to be more efficient than PhSeBr in the cyclization reactions. Key Words: Olefinic alcohols / Cyclofunctionalization / Benzeneselenenyl halides