Bulletin of the Chemical Society of Japan p. 861 - 868 (1988)
Update date:2022-07-29
Topics: Synthesis IR spectroscopy NMR spectroscopy Reactions Nucleophilic substitution Selenium dioxide Grignard Reagent Electrophilic Substitution Selenoketones Organoselenium Tertiary selenide
Ishii, Akihiko
Okazaki, Renji
Inamoto, Naoki
A new, convenient method for the synthesis of selenoketones has been reported.The reaction of dimagnesium salts of ketone hydrazones with diselenium dichloride affords an intermediate tentatively assigned as tetraselenides, which are converted into seleno
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Doi:10.1002/ardp.200800048
(2008)Doi:10.1021/jf0720279
(2007)Doi:10.1016/j.tet.2007.08.053
(2007)Doi:10.1039/J19680002673
()Doi:10.1246/cl.1984.1795
(1984)Doi:10.3184/174751912X13543818811749
(2013)