32363-44-3Relevant articles and documents
Conformational investigations of benzophenones by means of the Kerr effect and dipole moment methods
Bulgarevich, S. B.,Movshovich, D. Ya.,Ivanova, N. A.,Gruntfest, M. G.,Finocchiaro, P.,Failla, S.
, p. 259 - 268 (1994)
Molar Kerr constants and electric dipole moments are reported for differently substituted benzophenones (such as (4-FC6H4)2CO, (4-ClC6H4)(C6H5)CO, (4-MeC6H4)(C6H5)CO, (4-MeOC6H4)(C6H5)CO, (2-ClC6H4)(C6H5)CO, (2-MeC6H4)(C6H5)CO, (4-ClC6H4)(2',4',6'-Me3C6H2
Tunable aryl imidazolium recyclable ionic liquid with dual br?nsted-lewis acid as green catalyst for friedel-crafts acylation and thioesterification
Chen, Wen-Tin,Chou, Shih-Huan,Ho, Wen-Yueh,Hung, Ming-Wei,Lin, Michelle,Lin, Wesley,Lin, Yi-Jyun,Luo, Shun-Yuan,Reddy, Daggula Mallikarjuna,Thul, Mayur,Wu, Hsin-Ru,Wu, Yao-Peng
, (2020/01/28)
Unique tunable aryl imidazolium ionic liquids successfully catalyzed Friedel-Crafts acylation and thioesterification in sealed tubes. These reactions can form a C-C bond and a C-S bond with high atom economy. Ionic liquids exhibited high activity and catalyzed essential reactions with good to excellent yields while retaining their catalytic activities for recycling.
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.
