250686-92-1Relevant academic research and scientific papers
Catalytic Friedel-Crafts acylation: Magnetic nanopowder CuFe 2O4 as an efficient and magnetically separable catalyst
Parella, Ramarao,Naveen,Kumar, Amit,Babu, Srinivasarao Arulananda
, p. 1738 - 1742 (2013/03/28)
Catalytic regioselective Friedel-Crafts acylation of an array of anisoles/arenes with various acid chlorides using 5-20 mol % of magnetic nanopowder CuFe2O4 is reported. Unlike the conventional Friedel-Crafts reactions, which are catalyzed by moisture sensitive homogeneous catalysts/promoters, the nanopowder CuFe2O4 catalyst is moisture insensitive and the product/ketone-catalyst isolation is easily achieved using the magnetic properties of CuFe2O4.
LATERALLY SUBSTITUTED 4-n-ALKYLPHENYL 4-n-ALKYLBICYCLO(2. 2. 2)OCTANE-1-CARBOXYLATES.
Gray,Kelly
, p. 109 - 119 (2007/10/02)
Different substituents (fluoro, chloro, bromo, and cyano) have been separately introduced into the 2-position of the phenolic moiety of the 4-n-alkylphenyl 4-n-alkylbicyclo(2. 2. 2)octane-1-carboxylates to produce new series of low melting esters with lar
