117901-63-0Relevant academic research and scientific papers
Cleavage of Cyclic Ethers Including Oxetane and Oxolane with a Highly Nucleophilic Species of Phenylselenide Anion
Haraguchi, Kazuhiro,Tanaka, Hiromichi,Hayakawa, Hiroyuki,Miyasaka, Tadashi
, p. 931 - 934 (1988)
Phenylselenide anion generated from (PhSe)2 and LiAlH4 was found to be highly reactive to various types of cyclic ethers, providing a new method to prepare γ- and δ-phenylselenenyl alcohols from oxetane and oxolane, respectively.
Preparation of γ- and δ-Phenylselenyl Alcohols via Ring Cleavage of Oxetane and Oxolane
Haraguchi, Kazuhiro,Tanaka, Hiromichi,Miyasaka, Tadashi
, p. 434 - 436 (2007/10/02)
Various types of oxetanes and oxolanes can be cleaved by reaction with phenylselenide anion prepared from diphenyl diselenide and lithium aluminum hydride in dioxane.
