96818-49-4Relevant academic research and scientific papers
Stereoselective Synthesis of Z-Vinyl Selenides Through the Reaction of Sodium Selenide with Organic Halides and Alkynes
Pistoia, Renan P.,Back, Davi F.,Zeni, Gilson
, p. 3794 - 3798 (2019)
A practical synthetic approach to the stereoselective synthesis of Z-vinyl selenides is described through the reaction of sodium selenide with organic halides, followed by the addition to alkynes. The reaction conditions were also successfully applied to
Pyridylseleno Group in Organic Synthesis. Part 4. Oxyseleniation of Olefins using Pyridine-2-selenenyl Bromide as a Selenium Reagent and its Utilization in the Synthesis of 2-Pyridyl Vinylic Selenides
Toshimitsu, Akio,Owada, Hiroto,Terao, Keiji,Uemura, Sakae,Okano, Masaya
, p. 373 - 378 (2007/10/02)
The reaction of olefins with pyridine-2-selenenyl bromide in methanol as solvent affords β-methoxyalkyl 2-pyridyl selenides (A) in good to excellent yields.This reaction also proceeds in acetic acid and aqueous tetrahydrofuran to give acetoxyseleniated an
