A method for the degradation of pyrrolidine in water is described. The method relaies on the photocatalytic degradation of pyrrolidine to CO2 and NH3 by UV irradiation and using titanium dixide semiconductor as a photocatalyst. Compared with direct photolysis, the semiconductor catalytic photolysis gave consistently higher degradation yields for pyrrolidine in water. T...

Electron spin resonance spectroscopy (ESR) studies on the reduction process of nitroxyl spin probes were carried out for 1mM concentration of 14 N-labeled pyrrolidine nitroxyl spin probes, 3-carbamoyl-2,2,5,5-tetramethyl-pyrrolidine-1-oxyl (carbamoyl-PROXYL) and 3-carboxy-2,2,5,5-tetramethyl-pyrrolidine -1-oxyl (carboxy-PROXYL), 14 N-labeled piperidine nitroxyl spin probes, 4-methoxy-2,2,6,6-te...

In the title compound, C(11)H(19)NO(5), the five-membered pyrrolidine ring adopts an envelope conformation. The dihedral angles between the carboxyl group plane, the pyrrolidine ring and the meth-oxy group are 59.50 (3) and 62.02 (1)°, respectively. In the crystal, inter-molecular O-H⋯O hydrogen bonds link the mol-ecules into chains along [100]. The absolute configuration is assigned in accord ...

The reaction of pyridyl-1-azaallyl germanium(ii) chloride RGeCl () [R = {N(SiMe(3))C(Ph)C(SiMe(3))(C(5)H(4)N-2)}] with lithium metal afforded the dimeric germanium(i) compound [(RGe)(2)] (); compound reacts with an excess of elemental sulfur to afford the novel germanium analogue of a dithiocarboxylic acid anhydride [{Ge(S)R}(2)S] () via the insertion of elemental sulfur into the Ge(i)-Ge(i) bo...

a new, high yielding method for the preparation of vasicinone (7) is described. reaction of 2-nitrobenzoic acid with n, n¢-carbonyldiimidazole followed by 2-pyrrolidinone gave 1-(2-nitrobenzoyl)pyrrolidine-2-one (3). reduction of the latter with 10% pd-c afforded deoxyvasicinone (4). reaction of deoxyvasicinone (4) with bromine yielded monobromo-deoxyvasicinone (5). exchange of bromine of 5 wit...

An alternative and practical synthesis of (S)-1-(2-chloroacetyl)pyrrolidine-2-carbonitrile was achieved. Reaction of L-proline with chloroacetyl chloride was followed by conversion of the carboxylic acid moiety of the resulting N-acylated product into the carbonitrile via the corresponding amide intermediate. The synthesized pyrrolidine derivative was utilized to prepare DPP-IV inhibitor Vildag...

Macrophage inflammation and foam cell formation are critical events during the initiation and development of atherosclerosis (AS). C1q/tumor necrosis factor-related protein-3 (CTRP3) is a novel adipokine with anti-inflammatory and cardioprotection properties; however, little is known regarding the influence of CTRP3 on AS. As macrophages play a key role in AS, this study investigated the effect...

In studies on the metabolism of randomly labeled ( -)-nicotine-C4 in the anesthetized dog, it has been observed (2, 3) that the major part of the administered radioactivity, approximately 80 to 90$&, appears in the urine. Approximately one-tenth of this radioactivity is present as nicotine. From various experiments in which unlabeled (-)-nicotine and one of its metabolites, (-)-cotinine, have b...

www.experimentjournal.com 1254 Synthesis, biological activity and docking studies of N,N'-(3S,4S)bis(3,4-disubstituted pyrrolidine)-1-sulfonamide derivatives as β-gluscosidase inhibitors Abstract Starting with L-tartaric acid the chiral 3,4-disubstituted pyrrolidine analogue sulfonamide derivatives were prepared. These compounds were examined for anti-bacterial and anti-fungal activity. Further...