105423-62-9Relevant academic research and scientific papers
2-(4-Chlorophenylseleno)-2-butenal as a New Dienophile for Diels-Alder Reaction
Uneyama, Kenji,Takano, Kunikazu,Torii, Sigeru
, p. 2867 - 2868 (1983)
Diels-Alder reaction of 2-(4-chlorophenylseleno)-2-butenal with butadiene, isoprene, trans-1,3-pentadiene, and cyclopentadiene provided the corresponding adducts in 80-90percent yields, which were subsequently transformed into cyclohexadienal derivatives.
Preparations de composes α-arylselenocarbonyles a l'aide de morpholinoareneselenenamides
Lerouge, Patrice,Paulmier, Claude
, p. 1219 - 1224 (2007/10/02)
The reactivity of the morpholinoareneselenenamides 1 which are readily prepared from various diaryldiselenides, is investigated.The selenenamides 1 are good α-selenenylating agents for aliphatic aldehydes, α-ketoesters and conjugated enals yielding the α-
ELECTROCHEMICAL HYDROXYSELENENYLATION AS A NEW METHOD FOR ONE-STEP PREPARATION OF α-ARYLSELENO-α,β-UNSATURATED ALDEHYDES FROM 3-HYDROXYALKYNES
Uneyama, Kenji,Takano, Kunikaju,Torii, Sigeru
, p. 1161 - 1164 (2007/10/02)
Electrochemical oxidation of 3-hydroxyalkynes in the presence of diaryl diselenides in MeCN-H2O provided α-arylseleno-α,β-unsaturated aldehydes 2 in 62-94percent yields via hydroxyselenenylation of alkynes.
