56620-97-4Relevant academic research and scientific papers
Oxovanadium(V)-induced vicinal dialkylation of cyclic enones with organozinc compounds
Hirao, Toshikazu,Takada, Takashi,Sakurai, Hidehiro
, p. 3659 - 3661 (2000)
(matrix presented) Oxovanadium(V) compounds induce nucleophilic α,β-vicinal dialkylation of cyclic α,β-enones with dialkylzinc reagents. Alkylzinc enolates generated from cyclic enones and lithium trialkylzincates were also oxidized by VO(OEt)Cl2, giving 2,3-dialkylcycloalkanones.
SYNTHETIC APPLICATIONS OF 2-PHENYLSELENENYLENONES-III AN OVERVIEW
Liotta, Dennis,Saindane, Manohar,Barnum, Christopher,Zima, George
, p. 4881 - 4890 (2007/10/02)
2-Phenylselenenylenones are versatile species which can be selectively converted a number of different ketones and enones in high overall yields.
