5292-53-5Relevant articles and documents
Bifunctional acid-base ionic liquid organocatalysts with a controlled distance between acid and base sites
Boronat, Mercedes,Climent, Maria J.,Corma, Avelino,Iborra, Sara,Monton, Raquel,Sabater, Maria J.
, p. 1221 - 1231 (2010)
Bifunctional acid-base ionic liquid organocatalysts with different distances between the two sites have been synthesised, and their activity for the Knoevenagel condensation has been tested. As has been found to be the case with enzymes, the distance betw
Synthesis, characterization, and catalytic activity of ionic liquids based on biosources
Moriel,García-Suárez,Martínez,García,Montes-Morán,Calvino-Casilda,Ba?ares
, p. 4877 - 4881 (2010)
New room-temperature ionic liquids were synthesized from natural and easily available feedstocks (choline hydroxide and amino acids) following an economical and green route in which the only by-product was water. They were successfully applied as catalyst
Mg/Al-CO3 layered double hydroxide nanorings
Yang, Miaosen,Liu, Junfeng,Chang, Zheng,Williams, Gareth R.,O'Hare, Dermot,Zheng, Xuehan,Sun, Xiaoming,Duan, Xue
, p. 14741 - 14746 (2011)
Mg/Al-CO3 Layered Double Hydroxide (LDH) nanorings with a 750 nm exterior diameter and 250 nm interior diameter were synthesized in an organic/water solvent system via a urea hydrolysis method, using Mg 10(OH)18Cl2/s
Alkaline carbons as effective catalysts for the microwave-assisted synthesis of N-substituted-gamma-lactams
Calvino-Casilda,Martín-Aranda,López-Peinado
, p. 73 - 81 (2011)
The selective construction of new CC or Cheteroatom bonds is frequently the fundamental step in the synthesis of derivatives with high added value. In particular, molecules with CN bonds are of great interest due to their widespread use and intrinsic impo
Highly Active Bisamino Functionalized Zr(IV)-UiO-67 Metal-Organic Framework for Cascade Catalysis
Das, Aniruddha,Anbu, Nagaraj,Mostakim,Dhakshinamoorthy, Amarajothi,Biswas, Shyam
supporting information, p. 2830 - 2834 (2020/07/04)
This work reports the synthesis and characterization of Zr(IV)-based UiO-67-(NH2)2 (called 1) metal-organic framework. Activated 1 (named 1') was shown to be an efficient tandem catalyst in the conversion of benzaldehydedimethyl acet
Johnson-Corey-Chaykovsky fluorocyclopropanation of double activated alkenes: Scope and limitations
Kazia, Armands,Melngaile, Renate,Mishnev, Anatoly,Veliks, Janis
supporting information, p. 1384 - 1388 (2020/03/03)
Johnson-Corey-Chaykovsky fluorocyclopropanation of double activated alkenes utilizing S-monofluoromethyl-S-phenyl-2,3,4,5-tetramethylphenylsulfonium tetrafluoroborate is an efficient approach to obtain a range of monofluorocyclopropane derivatives. So far, fluoromethylsulfonium salts have displayed the broadest scope for direct fluoromethylene transfer. In contrast to more commonly used fluorohalomethanes or freon derivatives, diarylfluoromethylsulfonium salts are bench stable, easy-to use reagents useful for the direct transfer of a fluoromethylene group to alkenes giving access to the challenging products-fluorocyclopropane derivatives. Interplay between the reactivity of the starting materials and stability of the fluorocyclopropanes formed determines the outcome of the process.