Mixed anhydrides with penicillinic acids (III) were unstable and gave N-acyl, amides IV. Only III with butyrolactam was stable and reacted with alcohols to give esters V. All anhydrides with cephalosporinic acids (VIlI) yielded symmetric anhydrides IX. Alcoholysis of IX gave cephalosporinic ester X, while aminolysis yielded amide. Formation of postulated isomeric mixed anhydride with O-imino ca...

The mechanism that has been proposed for glyoxalase II [36] is summarized in Figure 3. It involves direct nucleophilic attack of an active-site histidine on the thiol ester substrate to form an acyl-imidazole intermediate which then rapidly hydrolyses. This is consistent with the known susceptibility of thiol esters to aminolysis and with the lability of acyl-imidazoles [47].

here, in situ synthesis of nano zinc oxide, along with aminolysis of polyester fabric, has simultaneously been carried out by using triethanol amine (tea) and zinc acetate. the zno nano particles (nps) were formed and stabilized on the fabric surface by amine compound at 130 °c for 1 h. the synthesis of nano zno particles on the polyester fabric were confirmed by x-ray diffraction (xrd) pattern...

Dicationic sandwich complexes containing thiophene, 2-methylthiophene7 2,5-dimethylthiophene, and tetramethylthiophene react with ammonia to give salts of the formula [(ring)Ru(SC4R4NH2)lX where ring = CsMe6 or cymene. The thiophene, 2-methylthiophene, and 2,5-dimethylthiophene complexes undergo C-S cleavage to give iminium-thiolato derivatives. In the case of the 2,5-dimethylthiophene complex,...

Azetidine is a prevalent structural motif found in various biologically active compounds. In this research paper, we report La(OTf) 3 -catalyzed intramolecular regioselective aminolysis of cis -3,4-epoxy amines to afford azetidines. This reaction proceeded high yields even the presence acid-sensitive and Lewis basic functional groups.

In this work, a series of novel paraffin inhibitor, polyaminoamide (PAA), was designed and prepared by aminolysis and poly-condensation using soybean oil and canola oil as the raw material. The property of the PAAs as paraffin inhibitor was investigated, the results show several PAA samples are potent in paraffin inhibition, and PPC-2 is the most effective one. Besides, the paraffin crystal mor...

Five active pharmaceutical ingredients (APIs) containing the vicinyl amino alcohol moiety were synthesized using a convergent chemical assembly system. The continuous system is composed of four flow reaction modules: biphasic oxidation, Corey-Chaykovsky epoxidation, phenol alkylation, and epoxide aminolysis. Judicious choice of reagents and module order allowed for two classes of β-amino alcoho...

[formula: see text] Aminocyclodextrins (ACDs), perfunctionalized at the 6-position with amino groups, bind phosphonoformate (PFA) diesters and accelerate acyl transfer reactions with high efficiency at neutral pH. Aminolysis and esterolysis are accelerated and hydrolysis of PFA diesters is catalyzed by ACDs. PFA diesters have significant antiviral activity. The rapid reactions observed with ACD...

The kinetic enzymatic resolution of azo acetates via aminolysis with Candida antarctica lipase B has been investigated using benzylamine as amine component. The products obtained from this biotransformation in high enantiomeric purity can serve as valuable precursors for various amino alcohols, as exemplified by the synthesis of the serotonin reuptake inhibitor (S)-(+)-cericlamine.