17315-86-5Relevant articles and documents
Green and selective toluene oxidation–Knoevenagel-condensation domino reaction over Ce- and Bi-based CeBi mixed oxide mixtures
Varga, Gábor,Kukovecz, ákos,Kónya, Zoltán,Sipos, Pál,Pálinkó, István
, p. 308 - 315 (2019/11/29)
Both Bi- and Ce-based CeBi mixed oxides were prepared by a modified sol-gel process from their precursor salts. The mixed as well as the parent oxides were characterized by X-ray diffractometry, Raman, XPS, UV–DRS and X-ray photoelectron spectroscopies, ICP–OES method, scanning and transmission electron microscopies as well as BET surface area, CO2- and NH3-temperature-programmed desorption measurements. After characterizing the morphology, the acid-base properties, the oxidation states of the cationic components and the porosity of these structures, their catalytic activities were probed in the Koevenagel condensation of benzaldehyde and diethyl malonate and the toluene oxidation to benzaldehyde reactions. Based on the catalytic activities of the oxides in the individual reactions, a catalyst mixture from the Bi- and Ce-based mixed oxides was used successfully in the toluene to benzaldehyde oxidation and benzaldehyde to benzylidene malonate Knoevenagel condensation domino reaction under environmentally benign conditions.
PROCESS FOR THE PREPARATION OF AN ARYL OXIME AND SALTS THEREOF
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Page/Page column 25; 26, (2013/05/09)
The invention relates to a process for the preparation of 3-cyano-3-{4-[(4-{[(2Z)-2-(methoxyimino)-2-phenylethyl] oxy} benzyl) oxy] phenyl} propanoic acid or salts thereof. In one form, the invention relates to the process for the preparation of (-)-3-cyano-3-{4-[(4-{[(2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenyl}propanoic acid and conversion of the (-)-enantiomer to the sodium salt, sodium 3-cyano-3-{4-[(4-{[(2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy] phenyl}propanoate.
First bovine serum albumin-promoted synthesis of enones, cinnamic acids and coumarins in ionic liquid: An insight into the role of protein impurities in porcine pancreas lipase for olefinic bond formation
Sharma, Nandini,Sharma, Upendra K.,Kumar, Rajesh,Katoch, Nidhi,Kumar, Rakesh,Sinha, Arun K.
scheme or table, p. 871 - 878 (2011/06/19)
During studies on exploiting the catalytic promiscuity of crude porcine pancreas lipase (PPL) in ionic liquid for C=C bond formations, bovine serum albumin (BSA) was found to be competing for these reactions. After a detailed investigation, we establish that these transformations are possible by unspecific protein catalysis rather than catalytic promiscuity of "PPL" - a first insight into the role of protein impurities in crude enzyme. Thus, a novel and highly efficient, environmentally friendly approach involving synergistic catalysis by bovine serum albumin-1-butyl-3- methylimidazolium bromide (BSA-[bmim]Br) has been developed for the synthesis of (E)-α,β-unsaturated compounds including a one-pot cascade synthesis of cinnamic acids and coumarins via aldol, Knoevenagel and Knoevenagel-Doebner condensations.
