10384-88-0Relevant academic research and scientific papers
Ionic liquids as a reusable media for copper catalysis. Green access to alkenes using catalytic olefination reaction
Muzalevskiy, Vasily M.,Shastin, Aleksey V.,Shikhaliev, Namiq G.,Magerramov, Abel M.,Teymurova, Aytekin N.,Nenajdenko, Valentine G.
supporting information, p. 7159 - 7163 (2016/10/24)
It was demonstrated that ionic liquids are superb recyclable media for copper catalyzed reactions using catalytic olefination reaction as an example. As a result a novel green access to the halogenoalkenes was elaborated. Possibility to perform up to five reaction cycles without catalyst leaching and decreasing of the yield was demonstrated. A number of various ionic liquids was screened and 1-butyl-3-methylimidazolium tetrafluoroborate ([bmim] [BF4]) was found the solvent with highest efficiency. Mild conditions, high atom economy comparing to other known methods, low amounts of wastes and possibility to recover ionic liquid are the advantages of the proposed method.
Synthesis of bis(halovinyl)benzenes by catalytic olefination
Muzalevskiy,Shikhaliev,Magerramov,Gurbanova,Geydarova,Balenkova,Shastin,Nenajdenko
, p. 678 - 682 (2014/01/23)
Catalytic olefination of hydrazines of terephthalic and isophthalic aldehydes with polyhaloalkanes afforded the corresponding p- and m-divinylbenzene derivatives bearing halogen atoms and various functional groups at the double bonds. Stereochemical featu
Conversion of aromatic aldehydes into 1-aryl-2,2-dichloroethenes
Nenajdenko,Shastin,Korotchenko,Balenkova
, p. 1047 - 1050 (2007/10/03)
A new general one-pot preparative method for the synthesis of 1-aryl(hetaryl)-2,2-dichloroethenes from aldehydes was developed. The method involves successive conversions of the latter into hydrazones followed by treatment with carbon tetrachloride in the
